Ralcorp Frozen Bakery Products Recalls Wal-Mart Bakery Brand Peanut Butter Cookies Because Of Possible Health Risk

FOR IMMEDIATE RELEASE -- Downers Grove, IL, January 18, 2009 -- Ralcorp Frozen Bakery Products, Inc. announced that it has taken the precautionary measure of voluntarily recalling all Wal-Mart Bakery brands of PEANUT BUTTER COOKIES, PEANUT BUTTER NO-BAKE COOKIES and PEANUT BUTTER FUDGE NO-BAKE COOKIES because they have the potential to be contaminated with Salmonella.  The cookies contain peanut butter supplied by Peanut Corporation of America which is the subject of an FDA investigation concerning recent Salmonella outbreaks. No illnesses have been reported in connection with the recalled cookies and no other type of Wal-Mart Bakery brand cookies are being recalled.

The recalled peanut butter cookies are distributed nationally under the Wal-Mart Bakery cookies brand. The recalled Wal-Mart Bakery no-bake peanut butter cookies and no-bake fudge peanut butter cookies were distributed nationally with the exception of the following states:  Wisconsin, Michigan, Minnesota, Illinois, Indiana, Ohio, Pennsylvania, Delaware, New Jersey, New York, Rhode Island, Connecticut, Massachusetts, Vermont, New Hamshire and Maine.  The cookies are sold in the in-store bakery sections of only Wal-Mart stores and have a code date of 9200 or less.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention’s Website at http://www.cdc.gov.

The FDA and other regulatory agencies have indicated that Peanut Corporation of America (PCA) is the focus of their investigation concerning a recent Salmonella outbreak thought to be caused by tainted peanut butter.  PCA supplied the Company with peanut butter it used in the recalled cookies.  The Company has been informed that the FDA continues its investigation as to what caused the problem with peanut butter supplied by PCA.

Consumers who have purchased any products covered by this recall are urged to return them to the store of purchase for a full refund.  Consumers with questions or concerns about the recall may call the 24-hour toll-free hotline at 1-888-421-4699.  Consumers with questions or concerns about their health should contact their doctor.

Peanut Corporation of America Expands Nationwide Recall of Peanut Butter
Company Announces the Voluntary Recall of Peanut Paste Produced in Georgia Plant

FOR IMMEDIATE RELEASE -- Lynchburg, Va. (January 18, 2009) -- Peanut Corporation of America (PCA), is expanding the recall of peanut butter and voluntarily recalling peanut paste made at its Blakely, Georgia facility because the products have the potential to be contaminated with Salmonella. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The recalled peanut butter and peanut paste were distributed to institutions, food service industries, and private label food companies in 24 states, the province of Saskatchewan in Canada, Korea and Haiti. The U.S. states are the following: Arkansas, California, Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Maryland, Michigan, Minnesota, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, Utah and Virginia. In addition, affected product was used as an ingredient in other products that may have been distributed in other states.

None of the peanut butter being recalled is sold directly to consumers through retail stores by PCA.

The recalled peanut butter in the expanded recall is sold by PCA in bulk packaging in containers ranging in size from five to 1,700 pounds. The peanut paste is sold in sizes ranging from 35-pound containers to tanker containers. The lot numbers for all recalled products are at the end of this news release. All of the peanut butter and peanut paste in the expanded recall was made on or after July 1, 2008, and only at the Georgia facility.

The potential for contamination was noted after a small number of samples from unopened containers and environmental samples from the Blakely, Georgia facility tested positive for Salmonella. The U.S. Food and Drug Administration has said the investigation is "very active and dynamic," and PCA continues to work closely with the FDA and the Centers for Disease Control and Prevention as they continue their investigation into the nationwide outbreak of Salmonella.

The Blakely, Georgia facility has currently stopped producing all products as the FDA and CDC continue their investigation, but some PCA staff remain to assist in the on-going investigation.

PCA is notifying customers that may have received the recalled product by phone and/or in writing. Customers should segregate and hold the product and call PCA at 1-877-564-7080 for further instructions. "We deeply regret that this product recall has expanded, and our first priority is to protect the health of our customers," said Stewart Parnell, President of Peanut Corporation of America.

The following is a list of all the products affected by the original recall and the amended recall:

Lot Numbers Affected:

8183 8184 8185 8186 8187 8188 8189 8190 8191 8192 8193 8194 8195 8196 8197 8198
8199 8200 8201 8202 8203 8204 8205 8206 8207 8208 8209 8210 8211 8212 8213 8214
8215 8216 8217 8218 8219 8220 8221 8222 8223 8224 8225 8226 8227 8228 8229 8230
8231 8232 8233 8234 8235 8236 8237 8238 8239 8240 8241 8242 8243 8244 8245 8246
8247 8248 8249 8250 8251 8252 8253 8254 8255 8256 8257 8258 8259 8260 8261 8262
8263 8264 8265 8266 8267 8268 8269 8270 8271 8272 8273 8274 8275 8276 8277 8278
8279 8280 8281 8282 8283 8284 8285 8286 8287 8288 8289 8290 8291 8292 8293 8294
8295 8296 8297 8298 8299 8300 8301 8302 8303 8304 8305 8306 8307 8308 8309 8310
8311 8312 8313 8314 8315 8316 8317 8318 8319 8320 8321 8322 8323 8324 8325 8326
8327 8328 8329 8330 8331 8332 8333 8334 8335 8336 8337 8338 8339 8340 8341 8342
8343 8344 8345 8346 8347 8348 8349 8350 8351 8352 8353 8354 8355 8356 8357 8358
8359 8360 8361 8362 8363 8364 8365 8366 9001 9002 9003 9004 9005 9006 9007 9008
9009 9010 9011 9012 9013 9014 9015 9016

Lot Numbers Affected:
8169 8170 8172 8173 8174 8184 8185 8186 8187 8203 8204 8205 8206 8214 8215 8216
8217 8219 8220 8221 8222 8223 8225 8226 8227 8228 8259 8260 8261 8262 8263 8264
8280 8281 8282 8283 8302 8303 8304 8305 8308 8309 8310 8311 8343 8344 8345 8346
8347 8350 8351 8352

Ralcorp Frozen Bakery Products Recalls Lofthouse Peanut Butter Cookies, Chuck's Chunky Peanut Butter Cookies And Pastries Plus Gourmet Cookies Nationwide Because Of Possible Health Risk

FOR IMMEDIATE RELEASE -- Downers Grove, IL, January 18, 2009 -- Ralcorp Frozen Bakery Products, Inc. announced that it has taken the precautionary measure of voluntarily recalling its Lofthouse® brand PEANUT BUTTER COOKIES, PEANUT BUTTER NO-BAKE COOKIES and PEANUT BUTTER FUDGE NO-BAKE COOKIES, Parco Foods’ Chuck’s Chunky® food service brand PEANUT BUTTER COOKIES and Pastries Plus GOURMET COOKIES because the cookies have the potential to be contaminated with Salmonella.  The recalled cookies contain peanut butter supplied by Peanut Corporation of America which is the subject of an investigation concerning recent Salmonella outbreaks. No illnesses have been reported in connection with the recalled cookies. No other type of Lofthouse, Chuck’s Chunky or Pastries Plus brand cookies are being recalled.

The Lofthouse peanut butter cookies are sold in 12 count clear plastic clamshell containers while the peanut butter fudge no-bake cookies and the peanut butter no-bake cookies are sold in 9 or 12 count clear plastic clamshell containers.  The recalled Lofthouse cookies are sold nationally in the in-store bakery sections of grocery stores and other food retailers. The Parco Foods’ Chuck’s Chunky cookies are distributed nationally in 5lb boxes in the food service channels. The Pastries Plus gourmet cookies were sold in 21 count plastic containers in select club stores nationally.  All products will have a lot code of 9200 or less.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention’s Website at http://www.cdc.gov.

The FDA and other regulatory agencies have indicated that Peanut Corporation of America (PCA) is the focus of their investigation concerning a recent Salmonella outbreak thought to be caused by tainted peanut butter.  PCA supplied Ralcorp Frozen Bakery Products with the peanut butter it used in the recalled cookies, prompting the voluntary recall.  

\ Consumers who have purchased any products covered by this recall are urged to return them to the place of purchase for a full refund.  Consumers with questions or concerns about the recall may call the toll-free hotline at 1-888-421-4699.  Consumers with questions or concerns about their health should contact their doctor.

Ralcorp Frozen Bakery Products Recalls Food Lion Bake Shop Peanut Butter Cookies Nationwide Because Of Possible Health Risk

FOR IMMEDIATE RELEASE -- Downers Grove, IL, January 18, 2009. . .Ralcorp Frozen Bakery Products, Inc. announced that it has taken the precautionary measure of voluntarily recalling its Food Lion Bake Shop brand PEANUT BUTTER COOKIES because the cookies have the potential to be contaminated with Salmonella.  The recalled cookies contain peanut butter supplied by Peanut Corporation of America which is the subject of an investigation concerning recent Salmonella outbreaks. No illnesses have been reported in connection with the recalled cookies. No other type of Food Lion brand cookies are being recalled.

The recalled peanut butter cookies are distributed nationally under the Food Lion cookie brand Bake Shop. The Bake Shop peanut butter cookies are sold in 12 count clear plastic clamshell containers in the in-store bakery sections of Food Lion grocery stores. The products will have a lot code of 9200 or less.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention’s Website at http://www.cdc.gov.
The FDA and other regulatory agencies have indicated that Peanut Corporation of America (PCA) is the focus of their investigation concerning a recent Salmonella outbreak thought to be caused by tainted peanut butter.  PCA supplied Ralcorp Frozen Bakery Products with the peanut butter it used in the recalled cookies, prompting the voluntary recall.  

Consumers who have purchased any products covered by this recall are urged to return them to the place of purchase for a full refund.  Consumers with questions or concerns about the recall may call the toll-free hotline at 1-888-421-4699.  Consumers with questions or concerns about their health should contact their doctor.

South Bend Chocolate Company Recalls Various Candys Containing Peanut Butter Because of Possible Salmonella Contamination

FOR IMMEDIATE RELEASE -- January 18, 2009 -- The South Bend Chocolate Company today announced a voluntary recall of certain candy products because they contain peanut butter from Peanut Corporation of America, which may be contaminated with Salmonella.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention’s Website at http://www.cdc.gov. 

Candy impacted by the recall are all sold under The South Bend Chocolate Company brand name and were produced on or after July 1, 2008.  The candies under recall including:

• Assorted chocolates in 5 ounce (Product 121), 8 ounce (Product 122), 12 ounce (Product 123) and 26 ounce (Product 124) boxes  [Note the sugar free assorted chocolates are not affected, and are not part of the recall]
• Hoosiers in 5 ounce (Product 010, UPC# 4482300011) and 3.5 ounce (Product o11, UPC# 4482300010)
• Valentine Heart, 14 ounces (Product 1020)

The following products are also under recall and are sold to retail stores in bulk for sales of smaller quantities to their customers:

• 4.5lb Peanut Butter Fudge, Product 228
• 4 lb. Hoosiers, Product 410
• 5 lb. Peanut Butter Meltaway, Milk Chocolate, Product 204
• 5 lb. Peanut Butter Meltaways-Dark Chocolate, Product 204D
• 4.5lb Peanut Butter Chocolate Fudge, Product 229

Consumers who have purchased the recalled products are urged to return it to the store of purchase, or to destroy the product. Consumers with questions may contact The South Bend Chocolate Company at 574-233-2577.  Consumers with questions or concerns about their health should contact their health care professional.  Consumers with symptoms are urged to visit their health professional or to go to a hospital emergency room. 

The South Bend Chocolate Company, based in South Bend, Indiana, said it hasn’t found any problems or received any complaints about these products.  Mark Tarner, President of The South Bend Chocolate Company, said:  “we are taken these steps out of concern for our customers”.

Hy-Vee Inc. Recalls Bakery Products With Peanut Butter Distributed in Seven States Due to Possible Health Risk

FOR IMMEDIATE RELEASE -- WEST DES MOINES, IA -- January 17, 2009 -- Hy-Vee Inc. is voluntarily recalling the following products made in its bakery departments because they contain peanut butter that has the potential to be contaminated with salmonella: Peanut Butter Cookies, Monster Cookies, Peanut Butter Reese's Pieces Cookies, Peanut Butter Chocolate Chip Cookies, Lunchbox Reese's Pieces Cookies, Lunchbox Peanut Butter Cookies, People Chow Party Mix and Assorted Truffle Fudge. All sell-by dates are included in this recall. The products are sold in various packaging and quantities and have a Hy-Vee price label attached. All items should be destroyed or returned to Hy-Vee for a full refund.

The action was taken immediately after Peanut Corporation of America (PCA), the company that supplies bulk peanut butter to Hy-Vee, issued a recall of the peanut butter ingredient used to make the Hy-Vee bakery products. The recall is a precautionary step because of an unresolved nationwide outbreak of salmonella.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.  Healthy persons infected with salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare cases, infection with salmonella can result in the organism getting into the bloodstream and producing more severe illnesses, such as arterial infections (i.e. infected aneurysms), endocarditis and arthritis.

The identified items, sold in all Hy-Vee stores in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota and Minnesota, have not been directly linked to the salmonella outbreak and there have been no reported cases of the illness.

Hy-Vee Bakery Manufacturing of Des Moines, Iowa, supplies stores with many of their baked goods. PCA recalled a number of lots of the product this week after health inspectors found salmonella contamination in an already-opened container of peanut butter at a nursing home in Minnesota. Hy-Vee had been shipped product from two of the lots. Production was suspended immediately and stores instructed to remove baked goods that contained peanut butter from store shelves.

In addition, Hy-Vee has sent samples of the peanut butter to an independent lab for testing. Company officials emphasize that all these measures are precautionary and they are keeping close watch on the situation and FDA's efforts to find the source of the outbreak. Customers with questions should call their local store.

Recall -- Firm Press Release

FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.

Peanut Corporation of America Expands Nationwide Recall of Peanut Butter
Company Announces the Voluntary Recall of Peanut Paste Produced in Georgia Plant

FOR IMMEDIATE RELEASE -- Lynchburg, Va. (January 16, 2009) -- Peanut Corporation of America (PCA), a peanut processing company and maker of peanut butter for bulk distribution to institutions, food service industries, and private label food companies, today announced an expanded recall of peanut butter produced in its Blakely, Georgia processing facility as well as the voluntary recall of peanut paste produced in the same plant because these products have the potential to be contaminated with Salmonella. The company on January 13, 2009 previously announced the recall of 21 lots of peanut butter produced on or after July 1, 2008.

Today's announcement and voluntary recall affect all peanut butter produced on or after August 8, 2008 and peanut paste produced on or after September 26, 2008 at the Georgia facility. The peanut butter being recalled is sold by PCA in bulk packaging in containers ranging in size from five to 1,700 pounds. The peanut paste is sold in sizes ranging from 35 pound containers to tanker containers.

PCA is notifying customers who received the recalled product by telephone or in writing, as well as through the news media and a toll-free 24/7 hotline number. None of the peanut butter or peanut paste being recalled is sold directly by PCA to consumers through retail stores.

"Today, the FDA informed PCA that new product samples in unopened containers tested positive for Salmonella," said Stewart Parnell, President of Peanut Corporation of America.

The FDA has not yet confirmed the DNA fingerprints of these positive samples to match the strains causing the outbreaks of food borne illness in several states.

PCA is immediately stopping all production at the Blakely, Georgia facility and notifying its customers to recall and retain all affected product produced during these dates at this plant.

"We deeply regret that this product recall is expanding and our first priority is to protect the health of our customers. Our company has worked around the clock for the last week with federal regulators to help identify any potential problems. Our Blakely facility is currently not operating as we continue to work with federal food safety investigators,"Parnell said.

Customers should call 1-877-564-7080 for further instructions on what to do with the product or visit the company web site at www.peanutcorp.com.

Eating food contaminated with Salmonella can result in abdominal cramping, diarrhea, and fever. Most people infected with Salmonella develop the symptoms 12 to 72 hours after infection. The illness usually lasts 4 to 7 days, and most people recover with treatment. However, in some persons, the diarrhea may be so severe that the patient needs to be hospitalized. For more information on Salmonella bacteria, please visit the Centers for Disease Control and Prevention's Website at http://www.cdc.gov.

Peanut Corporation of America is a family-owned and operated business since 1976 based in Lynchburg, VA and operating facilities in Blakely, GA, Suffolk, VA and Plainview, TX. The company prides itself on the quality and freshness of its products and strives constantly to maintain an environment in compliance with federal, state and local regulations and guidelines to provide a clean, safe product. For more information, visit Peanut Corporation of America's Website at www.peanutcorp.com.

Recall -- Firm Press Release

FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.

Kellogg Company Announces Voluntary Nationwide Recall of Austin® and Keebler® Branded Peanut Butter Sandwich Crackers and Select Snack-Size Packs of Famous Amos® And Keebler® Soft Batch Peanut Butter Cookies Because of Possible Health Risk

FOR IMMEDIATE RELEASE -- BATTLE CREEK, Mich. -- January 16, 2009 -- Kellogg Company today announced a voluntary recall of certain Austin® and Keebler® branded Peanut Butter Sandwich Crackers and select snack-size packs of Famous Amos® Peanut Butter Cookies and Keebler® Soft Batch Homestyle Peanut Butter Cookies because the products have the potential to be contaminated with Salmonella. No other products are involved in this recall.

On January 14, Kellogg announced a precautionary hold on the sandwich crackers while FDA and other authorities investigated Peanut Corporation of America (PCA), one of Kellogg's peanut paste suppliers for these crackers. PCA has expanded their earlier recall to include peanut paste and peanut butter, prompting Kellogg to immediately announce this recall and to include the above- mentioned cookie and cracker products.

"The actions we are taking today are in keeping with our more than 100-year commitment to providing consumers with safe, high-quality products," said David Mackay, president and CEO, Kellogg Company. "We apologize for this unfortunate situation."

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention's Website at http://www.cdc.gov.

Consumers who have purchased the recalled products are urged to destroy the product. Consumers with questions or who would like a refund may contact the Kellogg Consumer Response Center at 877-869-5633. Consumers with questions or concerns about their health should contact their doctor.

Products impacted by the recall were produced on or after July 1, 2008, including:

• Austin® Quality Foods Cheese Crackers with Peanut Butter - all sizes
• Austin® Quality Foods Cheese & Peanut ButterSandwich Crackers – all sizes
• Austin® Quality Foods Mega Stuffed Cheese Crackers with Peanut Butter – all sizes
• Austin® Quality Foods PB & J Cracker Sandwiches – all sizes
• Austin® Quality FoodsSuper Snack Pack Sandwich Crackers
• Austin® Quality Foods Chocolate Peanut Butter Sandwich Crackers – all sizes
• Austin® Quality Foods Toasty Crackers with Peanut Butter – all sizes
• Austin® Quality Foods Reduced Fat Cheese & Peanut Butter Sandwich Crackers
• Austin® Quality Foods Reduced Fat Toasty Crackers with Peanut Butter Sandwich Crackers
• Austin® Quality FoodsCookie/Cracker Pack
• Austin® Quality FoodsVariety Pack
• Keebler® Cheese & Peanut Butter Sandwich Crackers – all sizes
• Keebler® Toast & PB'n J Flavored Sandwich Crackers – all sizes
• Keebler® Toast & Peanut Butter Sandwich Crackers – all sizes
• Famous Amos® Peanut Butter Cookies (2- and 3-ounce)
• Keebler® Soft Batch Homestyle Peanut Butter Cookies (2.5-ounce)

Salmonella-Tainted Peanut Butter Found in Connecticut

FOR IMMEDIATE RELEASE -- HARTFORD, January 16, 2009 – Food inspectors conducting recall effectiveness checks in the state this week in response to the nationwide salmonella outbreak linked to King Nut  peanut butter have confirmed the presence of salmonella bacteria in an unopened five-pound tub of peanut butter found at a Connecticut food distributor, Consumer Protection Commissioner Jerry Farrell, Jr.

“This is the first unopened tub of King Nut peanut butter found in the country that is definitively identified as being tainted with salmonella,” Farrell said.  “My office just received the results from the Connecticut Department of Public Health Laboratory confirming the presence of Salmonella Type B in an unopened tub.  This provides further evidence that some lots of King Nut brand peanut butter delivered to food service accounts are responsible for a recent outbreak of salmonella infections in consumers.”

The product, bearing one of the lot numbers identified in the recall, (lot # 8234 with a production date of 8/21/2008) was found at City Line distributors of West Haven.  It was the only tub of that recalled lot.  However, agency inspectors have taken samples of the other King Nut peanut butter tubs for analysis.

“City Line is cooperating fully with our agency, is sharing with us its distribution lists identifying where the other tubs of King Nut peanut butter were shipped, and we are contacting the appropriate health and consumer protection officials with this information,” Farrell said. “We believe that the peanut butter was distributed to a variety of locations in Connecticut, New York, Rhode Island and Mass., and we are going make sure the company takes appropriate action to prevent this product from being served.”

Peanut Corporation of America, the manufacturer of the King Nut peanut butter, recalled the product when it was informed that salmonella had been found in an open five-pound tub of King Nut peanut butter. All other King Nut products are safe and not included in this voluntary recall.

This product is not sold in retail stores, and therefore is unlikely to be in consumers’ homes. 

The Salmonella bacteria can cause an infection known as Salmonellosis, which often produces diarrhea, fever, and abdominal cramps 12 to 72 hours after infection. The illness usually lasts 4 to 7 days, and most persons recover without treatment. However, in some persons, the diarrhea may be so severe that the patient needs to be hospitalized. In these patients, the Salmonella infection may spread from the intestines to the blood stream, and then to other body sites and can cause death unless the person is treated promptly with antibiotics. Older adults, infants, and those with impaired immune systems are more likely to experience severe illness, and should be seen by a physician if they experience these symptoms.

Salmonella recovered from King Nut peanut butter by MDA lab found to be a genetic match to cases in national Salmonella outbreak

FOR IMMEDIATE RELEASE -- January 12, 2009 -- The Minnesota Departments of Agriculture and Health today announced that laboratory analyses have confirmed a genetic match between the strains of Salmonella bacteria found in a container of King Nut brand creamy peanut butter and the strains of bacteria associated with 30 illnesses in Minnesota and nearly 400 illnesses around the country.

MDA lab tests conducted last week discovered Salmonella bacteria in a 5-pound package of King Nut peanut butter collected from a long-term care facility associated with one of the reported illnesses.  The Minnesota Department of Agriculture (MDA) and the Minnesota Department of Health (MDH) issued a product advisory on Friday alerting institutions that may have received the product. MDA and MDH scientists performed additional testing this weekend to verify the connection between the contaminated product and the illnesses. 

State officials initially discovered the contaminated product through product testing conducted after MDH epidemiological evidence and an investigation by MDA’s Rapid Response Team implicated King Nut creamy peanut butter as a likely source of Salmonella infections in Minnesota residents. In the product advisory issued Friday, state officials urged establishments who may have the product on hand to avoid serving it, pending further instructions as the investigation progresses.

Eating food contaminated with Salmonella can result in abdominal cramping, diarrhea, and fever.  Anyone who believes they may have become ill as a result of eating this product or foods made with this product should contact their health care provider. 

King Nut peanut butter is produced by Peanut Corporation of America, of Lynchburg, Va., and is distributed in seven states by Ohio-based King Nut Companies. The product was distributed in Minnesota to establishments such as long-term care facilities, hospitals, schools, universities, restaurants, delis, cafeterias and bakeries. King Nut Companies reports that the product is not distributed for retail sale to consumers, and has voluntarily withdrawn the product from distribution.

Minnesota officials continue to coordinate their investigation with the Centers for Disease Control and Prevention, the U.S. Food and Drug Administration and other states. 

Perry's Ice Cream Company Announces Voluntary Recall of Select Peanut Butter Ice Cream Products Due to Possible Health Risk

FOR IMMEDIATE RELEASE -- Buffalo, N.Y. – January 17, 2009 – Perry’s Ice Cream today announced a voluntary recall of select ice cream products containing peanut butter because the products have the potential to be contaminated with Salmonella.

FDA and other regulatory agencies have indicated that Peanut Corporation of America (PCA) is the focus of an investigation concerning a recent Salmonella outbreak thought to be caused by tainted peanut butter. As a result of the investigation, PCA has recalled 170 lots of suspect peanut butter and peanut paste. PCA is one of Perry’s peanut butter sauce suppliers.

Perry’s is recalling ice cream products containing peanut butter sauce, which have been recalled by PCA. The company has not received any consumer illness complaints about these products. The products below have been distributed in New York, Pennsylvania, New Jersey, Maryland and Virginia.

Products affected by the recall are as follows:

ITEM DESCRIPTION

Perry's Premium Peanut Butter Cup Craze Ice Cream 1/2 Pint
Perry's Peanut Butter Cup Ice Cream 1.5 QT, 1.75 QT AND 3 GL
Perry's Peanut Butter Chip Frozen Yogurt 1.5 QT, 1.75 QT and 3 GL
Perry's Peanut Butter Sundae Crunch Ice Cream Bar Bulk 24 pack
Perry's Premium Peanut Butter Fudge Ice Cream 1.5 QT and 1.75 QT
Perry's Perfectly Churned Light Peanut Butter Cup Ice Cream 1.5 QT and 1.75 QT
Perry's Light Peanut Butter Cup Ice Cream 1.75 QT
Shurfine Peanut Butter Cup Ice Cream 1.75 QT
Wegmans Chocolate Nutty Cone Ice Cream 1.75 QT
Wegmans Peanut Butter Cup Ice Cream 1.75 QT and Pint
Wegmans Peanut Butter Swirl Ice Cream 1.75 QT
Wegmans Peanut Butter Sundae Ice Cream 1.75 QT
Wegmans Peanut Butter Pretzel Ice Cream 1.75 QT
Wegmans Peanut Butter Crunch Ice Cream Bar 6 pack
Wegmans Peanut Butter Candy Sundae Cup Ice Cream 4 pack
Wegmans Peanut Butter Sundae Cup Ice Cream 4 pack

"Product quality and consumer safety have been our top priority for over 90 years and our decision today reflects that tradition,” said Robert Denning, president and CEO, Perry’s Ice Cream. “We apologize for any inconvenience to our customers."

Salmonella is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. For more information on Salmonella, please visit the Centers for Disease Control and Prevention's Website at http://www.cdc.gov.

Consumers who have purchased the recalled products are urged to destroy the product. Consumers with questions or who would like a refund may contact the Perry’s Consumer Affairs Department at 1-800-873-7797 between the hours of 9:00 a.m. – 5:00 p.m., Monday through Friday EST. For updated recall information, or to leave a message during non-business hours, please call 716-562-0260.

Domega International Ltd., Inc Issues An Alert On Undeclared Sulfites In "Guangdayuan Brand Dried Sweet Potato"

FOR IMMEDIATE RELEASE -- December 31, 2008 -- DOMEGA INTERNATIONAL LTD., INC., of 98 Bay 35th Street, Brooklyn, NY 11214 is recalling “Guangdayuan Brand Dried Sweet Potato" because it contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.

The recalled "Guangdayuan Brand Dried Sweet Potato" is sold in an un-coded, clear 200 gram vacuum packed plastic bag and is a product of China. The product was sold nationwide.

The recall was initiated after routine sampling by NYS Department of Agriculture and Markets Food inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in “Guangdayuan Brand Dried Sweet Potato", which did not declare sulfites on the labels. The consumption of 10 milligrams of su1fites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.

No illnesses have been reported to date in connection with this product Consumers who have Purchased "Guangdayuan Brand Dried Sweet Potato", should return them to the place of purchase. Consumers with questions may contact the company at 1-646·938-734

Balanced Health Products, Inc. Expands Voluntary Urgent Nationwide Recall of Starcaps Dietary Supplement Capsules Found to Contain an Undeclared Drug Ingredient

FOR IMMEDIATE RELEASE -- December 8, 2008 -- Balanced Health Products, Inc. has expanded its voluntarily recall of STARCAPS DIET SYSTEM DIETARY SUPPLEMENT to include additional Lot Numbers 12/2009 – 82866 and 12/2010 - 83801, sold in 30 capsule plastic bottles.

The recall is effective immediately and is being undertaken because these lots of STARCAPS contain an undeclared drug ingredient- Bumetanide – a diuretic available by prescription only. Bumetanide is also not listed on the product label as an ingredient in this product.

Bumetanide is a diuretic indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease including nephrotic syndrome. Bumetanide has been detected in STARCAPS at a level of 0.8mg per capsule. Potential risks associated with the use of Bumetanide include serious and significant fluid and electrolyte loss and an elevation in uric acid concentrations. Consumers should not take Bumetanide if they are allergic to sulfonamides. Significant drug interactions with Bumetanide, such as with digoxin and lithium, may lead to an increase risk of toxicity. Patients may also be at an increased risk of hypotension (low blood pressure), fainting (syncope) and resultant injury if they have normal blood pressure or are already taking an antihypertensive medication and take STARCAPS with undeclared Bumetanide.

The company has received no reports of illness associated with this product.

The company’s investigation to date has indicated that an additional lot of raw material intended for use in the production of STARCAPS which has been stored in sealed drums since the time of its importation into the U.S. is also contaminated with Bumetanide. This information seems to indicate that the contamination occurred at the point of production of the raw material in Lima, Peru.

STARCAPS lot number 12/2009 – 82866, totaling 28,739 consumer-size bottles was distributed nationwide from 3/2006 to 4/2007 through retail outlets and online sales.

STARCAPS lot number 12/2010 - 83801, totaling 28,530 consumer-size bottles was distributed nationwide from 5/2007 to 7/2008 through retail outlets and online sales.

Consumers who purchased STARCAPS Lot Numbers 12/2009 – 82866 and 12/2010 – 83801 should immediately discontinue their use and return it to Balanced Health Products, Inc. at the address on the product label.

Consumers with questions may contact the company at (212) 794-9793 from 10:30am to 4pm EST Monday through Friday.

Consumers who experience adverse events with any lots of this product should seek immediate help from their physician or healthcare provider.

Retail stores are being notified by fax or registered mail to immediately stop all sales and return product to the company.

This recall is being made in cooperation with the US Food and Drug Administration.

Fashion Sanctuary Issues a Voluntary Nationwide Recall of All Lots of Zhen De Shou Fat Loss Capsules Found to Contain an Undeclared Drug Ingredient

FOR IMMEDIATE RELEASE --San Diego, CA -- November 23, 2008 --- Fashion Sanctuary is recalling all lot codes of Zhen De Shou Fat Loss Capsules sold in 10 count blister cards. The recall was initiated after notification by the Food and Drug Administration (FDA) that lab analysis of Zhen De Shou samples found the product to contain undeclared sibutramine, making it an unapproved drug. Sibutramine is an FDA approved drug used as an appetite suppressant for weight loss. This poses a potential threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

The product was primarily distributed in the U.S and sold via the Internet. It is sold in a box with an inner foil pouch. Inside the pouch is a blister pack containing light and dark green capsules. This recall affects all lot codes and use by dates. No illnesses or injuries have been reported to date in connection with this product.

Consumers who may have purchased product from this company should immediately discontinue using the product and contact the firm at zhendeshourecall@gmail.com to receive further instructions for returning the product or with any questions.

We sincerely regret any inconvenience to consumers. The firm has taken this voluntary action out of concern for the health and safety of consumers.

This recall is being made in cooperation with the US Food and Drug Administration.

Any adverse reactions experienced with the use of this product should also be reported to the FDA’s MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at wwww.fda.gov/medwatch.

Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops (Simethicone-Antigas) Non-Staining Due To Possible Metal Fragments

FOR IMMEDIATE RELEASE -- Fort Washington, PA (November 7, 2008) – Johnson & Johnson • Merck Consumer Pharmaceuticals Company (JJMCP) is voluntarily recalling approximately 12,000 units of Infants' MYLICON® GAS RELIEF DYE FREE drops (simethicone-antigas) non-staining sold in 1 oz. plastic bottles that were distributed after October 5, 2008 nationwide. The company is taking this action in consultation with the U.S. Food and Drug Administration (FDA). Although the potential for serious medical events is low, the company is implementing this recall to the consumer level as a precaution after determining that some bottles could include metal fragments that were generated during the manufacturing process. If any medical events were to occur, most are expected to be temporary and resolve without medical treatment. Parents who have given the product to their infant and are concerned should contact their health care provider immediately.

The two lots of Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining 1 oz. bottles included in the recall are:

Consumers can find the lot numbers on the bottom of the box containing the product and also on the lower left side of the sticker on the product bottle.

Consumers who purchased Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining included in this recall should immediately stop using the product and contact the company at 1-800-222-9435 (Monday – Friday, 8:00 a.m. – 8:00 p.m. EST) or via the internet at www.mylicon.com for instructions regarding how to dispose of the product and request a replacement or refund.

Infants' MYLICON® drops are sold over-the counter, in retail stores and pharmacies, as an anti-gas medicine to relieve the discomfort of infant gas frequently caused by air swallowing or by certain formulas or foods.

The recall does not affect any Original Infants' MYLICON® GAS RELIEF products (1/2 oz. or 1 oz. size) or Infants' MYLICON® GAS RELIEF DYE FREE drops non-staining (1/2 oz. size).

The manufacturer has instructed retailers and wholesalers to return their inventories.
 
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Nestlé Withdraws Nestlé Farinha Lactea Cereal in the United States

FOR IMMEDIATE RELEASE -- November 3, 2008 -- Nestlé is withdrawing Nestlé Farinha Lactea cereal in the United States. Nestlé is taking this action as we have learned that the product may contain residual traces of a pesticide not currently approved for use on wheat in the U.S. While the pesticide is approved for use in Brazil and the noted levels are well below Brazilian standards, it is not used on wheat products in the United States and therefore there is no set standard for its presence in cereal. The pesticide is permitted in the United States on grain crops other than wheat.

Nestlé Farinha Lactea cereal is manufactured in Brazil by Nestlé Brazil and sold primarily in Portuguese language communities in the United States. The withdrawal applies to all sizes, varieties and production codes of the product. No other Nestlé products are affected.

Nestlé USA is assisting with the withdrawal of this product from the U.S. market to ensure the continued quality and safety of Nestlé products. Nestlé has not received any illness reports or consumer complaints.

Consumers who have purchased Nestlé Farinha Lactea cereal should not consume the product, and should return it to the store where they purchased it for a full refund.

Amy’s Kitchen Inc. Issues Allergy Alert and Voluntary National Recall due to Possible Undeclared Milk in Tofu Scramble in a Pocket Sandwich; Lot Code H148

FOR IMMEDIATE RELEASE -- Santa Rosa, California, November 7, 2008. Amy's Kitchen Inc. of Santa Rosa, California is voluntarily recalling Tofu Scramble in a Pocket Sandwich Lot 10 H148, because of the presence of milk in a product that is labeled non-dairy. The 4.0 oz net wt frozen product, sold in U.S. grocery stores, comes in a retail package labeled as Amy's Tofu Scramble in a Pocket Sandwich. The code date printed in white on the easy open zipper end is

10 H148 A,B,C or D

The products could cause an allergic reaction if consumed by any individuals allergic to milk. People who have an allergy or severe sensitivity to dairy products run the risk of serious or life-threatening allergic reaction if they consume the product. Consumers without milk allergies can safely consume the product.

The recall was initiated after one report of an allergic reaction due to this product, which was not labeled as containing dairy ingredients. Testing has shown the presence of milk.

No other products or code dates of Amy's Kitchen products are affected by this recall.

Consumers allergic to milk should contact Amy's Kitchen for a replacement or refund. The product is distributed to retailers only. Retailers are instructed to destroy the affected product.

Amy's Kitchen is cooperating with FDA and will also issue an alert via the Food Allergy and Anaphylaxis Network.

For instructions or questions, consumers may call the company collect: 707-568-4500 and ask for the consumer services department at ext 4571. Consumers who are not allergic to milk ingredients can consume the product or call for a full refund.

Nonna's Real Italiana Cuccine Issues an Allergy Alert on Undeclared Milk, Soy, and Wheat in Stuffed Artichokes

FOR IMMEDIATE RELEASE -- October 22, 2008 -- Nonna's Real Italiana Cuccine of Slidell, LA is recalling the following Nonna's Real Italiana Cuccine brand products:

• Stuffed Artichokes, Net Wt. 15 oz.

This product is being recalled because it contains milk, soy, and wheat that was distributed in packaging that does not reveal the presence of these ingredients. People who have an allergy or severe sensitivity to milk, soy, or wheat run the risk of a serious or life-threatening allergic reaction if they consume these products.

This product is distributed through retailers in the Greater New Orleans area including the Northshore from October 8, 2008 to October 17, 2008. The product is individually wrapped in clear plastic wrap bearing the label: "STUFFED ARTICHOKE, Net Wt. 15 oz., NONNA'S REAL ITALIANA CUCCINE".

There have been no reported illnesses to date.

The above omission was found during a routine FDA inspection. Distribution of these products has been suspended while we correct the labels to include all ingredients.

Consumers who have questions or purchased the product may contact Ruby Lovecchio at 214-253-7630 for information and return instructions.

Arnold Foods Company, Inc. Issues Allergy Alert on Undeclared Nuts in Brownberry Whole Grains Bread 100% Whole Wheat

FOR IMMEDIATE RELEASE -- HORSHAM, PA, October 8, 2008 – Arnold Foods Company, Inc. is recalling BROWNBERRY brand Whole Grains BREAD 100% WHOLE WHEAT (1 LB 8 OZ) because it may contain undeclared almonds, walnuts and hazelnuts. People who have an allergy to these nuts run the risk of life threatening or serious allergic reactions if they consume the product.

The BROWNBERRY brand Whole Grains BREAD 100% WHOLE WHEAT was sold in Illinois, Indiana, Iowa, Minnesota and Wisconsin. This product was sold through retail stores and bakery thrift outlets.

The product being recalled has a green twist tie with a code date of "Oct 11" printed on the bread bag. No other Arnold brand or Brownberry brand products are affected.

The company announced the recall after receiving a report from one consumer who found nuts in the bread which are known allergens but were not listed on the ingredient statement. The company has received no other reports from consumers. There are no reports of injuries.

All packages with the above code date have been removed from store shelves.

Consumers with allergies to nuts who have purchased the product can return the product to its place of purchase for a full refund or call the company at 1-800-984-0989.

FDA Detects Melamine Contamination in Flavored Drink

The U.S. Food and Drug Administration (FDA) has increased inspections and product testing efforts in response to the melamine contamination problem which originated in Chinese dairy products.  As a result of the FDA’s on-going testing program, the agency has detected melamine contamination in Blue Cat Flavor Drinks.  The distributor of the product, Tristar Food Wholesale Co. Inc., initiated a recall of several flavors of Blue Cat Flavor Drink, based on the FDA’s findings.  The FDA advises the public not to consume this product and recommends that retailers and food service operators remove the product from sale or service.

Other Recalls

On September 26, the FDA issued an alert to consumers that seven Mr. Brown instant coffee and milk tea products were being recalled by the Taiwanese company, King Car Food Industrial Co. Ltd., due to possible contamination with melamine. King Car Food Industrial Co. used a non-dairy creamer manufactured by Shandong Duqing Inc., China, which was found to be contaminated with melamine. The recalled products are:

• Mr. Brown Mandheling Blend Instant Coffee (3-in-1)
• Mr. Brown Arabica Instant Coffee (3-in-1)
• Mr. Brown Blue Mountain Blend Instant Coffee (3-in-1)
• Mr. Brown Caramel Macchiato Instant Coffee (3-in-1)
• Mr. Brown French Vanilla Instant Coffee (3-in-1)
• Mr. Brown Mandhling Blend instant Coffee (2-in-1)
• Mr. Brown Milk Tea (3-in-1)

The FDA recommends that consumers not consume any of the above Mr. Brown instant coffee and milk tea products. The FDA also recommends that retailers and foodservice operators remove the products from sale or service.

Sunny Maid Corp. Monterey Park, Calif., who is an importer and distributor of Mr. Brown Instant Coffee products, is recalling the products in the United States.

The FDA is working with regulatory agencies in the United States as well as with other countries. The California Department of Public Health and the New Zealand Food Safety Authority reported that its testing of White Rabbit Creamy Candies has shown melamine contamination at high levels. In light of the widespread contamination of milk and milk-based products in China and the New Zealand Food Safety Authority’s finding, the FDA continues to recommend that consumers not eat White Rabbit Creamy Candy and that retailers and foodservice operations remove the product from sale or service.

A recall by QFCO Inc., Burlingame, Calif., of the White Rabbit Creamy Candies, is underway in the United States.

The FDA is closely monitoring these recalls and will continue to perform follow up activities of other recalls that may develop.

To date, the FDA is not aware of any illnesses in the United States stemming from consumption of Blue Cat Flavor Drinks, White Rabbit Creamy Candy, or the Mr. Brown instant coffee and milk tea products.

Individuals who have experienced any health problems after consuming Blue Cat Flavor Drinks, White Rabbit Creamy Candy, or any of the identified Mr. Brown coffee and tea products are advised to contact their health care professional.

Background

On September 12, 2008, in light of reports from China of melamine contaminated infant formula, the FDA issued a Health Information Advisory to assure the American public that there is no known threat of contamination in infant formula manufactured by companies that have met the requirements to sell such products in the United States.  That advisory also warned members of Chinese communities in the United States that infant formula manufactured in China, possibly available for purchase at Asian markets, could pose a risk to infants.

The FDA had contacted the companies who manufacture infant formula for distribution in the United States and received, from the companies, information that they are not importing formula or sourcing milk-based materials from China. 

At the same time, the FDA—in conjunction with state and local officials—began a nation-wide investigation to check Asian markets for Chinese manufactured infant formula that may have been brought into the United States. In particular, this effort focused on areas of the country with large Chinese communities, such as Los Angeles, San Francisco, Seattle and New York.  To date, investigators have visited more than 1,800 retail markets and have not found Chinese infant formula present on shelves in these markets.

The FDA also advises consumers not to purchase infant formula manufactured in China from Internet sites or from other sources. 

The FDA has taken, and will continue to take, proactive measures to help ensure the safety of the American food supply.  In conjunction with state and local officials, the FDA will continue to visit Asian markets for food items that are imported from China and that could contain a significant amount of milk or milk proteins.  In addition, the FDA has broadened its domestic and import sampling and testing of milk-derived ingredients and finished food products containing milk, such as candies, desserts, and beverages that could contain these ingredients from Chinese sources.  Milk-derived ingredients include whole milk powder, non-fat milk powder, whey powder, lactose powder, and casein.

In addition to state and local governments, the FDA is working in close cooperation with Customs and Border Protection within the U.S. Department of Homeland Security, the U.S. Department of Agriculture, Centers for Disease Control and Prevention, other federal agencies, and foreign governments.

#

Interim Safety and Risk Assessment of Melamine and Its Analogues in Foods for Humans

Questions and Answers

Melamine Methodology:

• Determination of Melamine and Cyanuric Acid Residues in Infant Formula using LC-MS/MS
• Interim Method for Determination of Melamine and Cyanuric Acid Residues in Foods using LC-MS/MS

Additional Information

FDA Updates Health Information Advisory on Melamine Contamination (Sept. 26, 2008)
FDA Updates Health Information Advisory on Melamine Contamination (Sept. 23, 2008)
FDA Updates Health Information Advisory on Melamine Contamination (Sept. 20, 2008)
FDA Issues Health Information Advisory on Infant Formula (Sept. 12, 2008)

Mr. Brown 3-In-1 & and 2-In-1 Powdered Packets in Bag Coffee Mixes Due To Health Risk (Oct. 1, 2008)
QFCO, Inc. Recalls White Rabbit Candy Because of Possible Health Risk (Sept. 26, 2008)

Consumer Alert: Undeclared Sulfites in "Shad Raisins"

FOR IMMEDIATE RELEASE -- October 6, 2008 -- New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Fatima Brothers Inc. of 54-08 43rd St Maspeth, New York 11378 is recalling "Shad Raisins" due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.

The recalled "Shad Raisins" were packaged in uncoded, 7-ounce plastic bags. "Shad Raisins" were distributed in New York City.

Routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the product contained high levels of sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.

No illnesses have been reported to date to this Department in connection with this product. Consumers who have purchased "Shad Raisins" should return them to the place of purchase.

Mom's Food Products, Inc. Issues Allergy Alert On Undeclared Eggs in Sandwiches and Potato Salad

FOR IMMEDIATE RELEASE -- September 23, 2008 -- Mom's Food Products, Inc. of Ft Worth, TX is recalling all Tuna Salad sandwiches, Pimento Cheese sandwiches, and potato salad because they may contain eggs in the salad dressing.  People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.

Product was distributed in the Texas area through retail stores or direct delivery. 

The tuna salad and pimento cheese sandwiches are packaged in black plastic wedges and the potato salad is in clear round containers included as part of Mom's Big Sub sandwich packages.

There have been no illnesses reported to date.

The recall was initiated after it was discovered that an ingredient change in salad dressing was not reported by Mom's supplier.

The products involved are:
Mom's Pimento Spread 5.0 oz black wedge (UPC 83898 00114)
Race Trac Pimento Spread 5.0 oz black wedge (UPC 83898 00114)
Crosby Food & Vending Pimento Spread 5.0 oz black wedge (UPC 83898 00114)
Outtakes Pimento Spread 4.0 oz black wedge (No UPC)
Mom's Tuna Salad 5.0 oz black wedge (UPC 83898 00108)
Race Trac Tuna Salad 5.0 oz black wedge (UPC 83898 00108)
2 Podner's Tuna Salad 5.0 oz Clam shell (UPC 83898 00108)
Canteen (Outtakes) Tuna Salad Croissant 4.5 oz Poly Sealed (No UPC)
Mom's Big Sub with 4.0 oz Potato Salad round opaque container (No UPC)

Consumers who have purchased these items are urged to return it to the place of purchase for a full refund.  Consumers with questions may contact Mom's Food Products at 1-800-743-0010.

K-Fat Inc. Issues Alert On Undeclared Sulfites In "Mut Gung Sweetened Ginger"

FOR IMMEDIATE RELEASE -- Brooklyn, NY -- September 12, 2008 --- K-FAT INC. of 13 Meadow St., Brooklyn, NY 11206, is recalling its 150g packages of MUT GUNG SWEETENED GINGER because they contain undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious life-threatening allergic reactions if they consume this product.

The product comes in a 150g clear plastic container. The recalled Mut Gung Sweetened Ginger was distributed nationwide in retail stores and through mail orders.

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 150g packages of Mut Gung Sweetened Ginger which were not declared on the label.  The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon digesting 10 milligrams or more of sulfites.  Analysis of the Mut Gung Sweetened Ginger revealed they contained 94.5 mg per serving.

No illnesses or allergic reactions involving this product have been reported to date. Consumers who have purchased 150g packages of Mut Gung Sweetened Ginger are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (718) 381-0306.

August 19 2008

There are often advantages to being old and walking around to keep the muscles from stiffening up, plus having hearing that is better then people think. Today while walking around Marina De Ray looking at the boats I heard the following being discussed on a cell phone on speaker by two overly dressed white haired men walking in front of me.

"Let him win, we will drag him thru the courts on inauguration day over the clause NATURAL BORN CITIZEN IN THE CONSTITUTION and cause a constitutional crisis like Bush caused when he stole the election from Gore. Nancy Pelosi will then become the first women president of the United States while the supreme court decides that McCain has a right to be president"

"The World will know that McCain's court stole the election for him like it did for Bush and we will be the winners pr wise."

This statement caused me to go check the law books and this is what I found covering the topic

John McCain, who ran for the Republican party nomination in 2000 and is the presumptive Republican nominee in 2008, was born at the Coco Solo U.S. military base in the Panama Canal Zone to U.S. parents. Although the Panama Canal Zone was not considered to be part of the United States, federal law states that "Any person born in the Canal Zone on or after February 26, 1904, and whether before or after the effective date of this chapter, whose father or mother or both at the time of the birth of such person was or is a citizen of the United States, is declared to be a citizen of the United States The law that conferred this status took effect on August 4, 1937, one year after John McCain was born — albeit with retrospective effect, resulting in McCain being declared a U.S. citizen from birth.

Congress apparently interpreted this clause when it enacted the first naturalization law on March 16, 1790:

"And the children of citizens of the United States that may be born beyond sea, or outside the limits of the United States, shall be considered as natural born citizens."

While this is the law of the land it not the law of the constitution of the United States of America and it is the constitution not congressional law that the president is elected under.

And those who are intratextually minded are likely to consider the Fourteenth Amendment, which provides:

"All persons born or naturalized in the United States, and subject to the jurisdiction thereof, are citizens of the United States and of the State wherein they reside."

The 14th amendment did not address the natural born citizen clause in the constitution which leaves a McCain presidency up to the supreme court if elected

Were these men for real or where they just blowing off steam that is up to you to decide but they did sound like they were pissed off and democrats have been looking to get even for the Gore loss and this gives a natural opportunity to do such.

FDA Warns Consumers Not to Eat Certain Mussel Products from Bantry Bay Seafood

The U.S. Food and Drug Administration (FDA) is warning consumers against eating certain frozen cooked mussel products made by Bantry Bay Seafoods, imported from Ireland, because they may be contaminated with azaspiracid toxins, a group of naturally occurring marine toxins known to cause nausea, vomiting, diarrhea, and stomach cramps.

Azaspiracid toxins are odorless, tasteless, and cannot be destroyed or neutralized by freezing or cooking, including boiling. Individuals who have experienced gastrointestinal symptoms such as those noted above after eating any of the products listed below should consult their health care professional. Symptoms typically occur within hours of consumption and persist for two to three days.

In July, two people in Washington state became ill after eating the company's "Mussels in a Garlic Butter Sauce." FDA tested unopened product from the same production lot and found that it contained the azaspiracid toxins.

Consumers should throw out the following Bantry Bay Seafood frozen cooked products with "Best before end" dates ranging from January 23, 2009, to November 15, 2009:

• Mussels in a Garlic Butter Sauce
• Mussels in White Wine Sauce
• Mussels in Tomato and Garlic Sauce

The "Best before end" dates are displayed on the side of the box in the following format: MM:DD:YY. Products to be thrown out are marked with dates 01:23:09 through 11:15:09.

These products are sold frozen in 1 pound cardboard packages in stores throughout the United States.

The FDA also recommends that retailers and foodservice operators remove these products, and any food in which these products were used as an ingredient, from sale or service.

Azaspiracid toxins were an unknown marine toxin until 1995, when they were identified and linked to an outbreak of foodborne illnesses associated with consumption of Irish shellfish. The toxins have since been identified in other shellfish from the west coast of Europe. They have never been detected in shellfish harvested from U.S. waters.

FDA Extends Consumer Warning on Serrano Peppers from Mexico

Laboratory testing by the U.S. Food and Drug Administration has confirmed that both a sample of serrano pepper and a sample of irrigation water collected by agency investigators on a farm in the state of Tamaulipas, Mexico (business address is in Nuevo Leon, Mexico) contain Salmonella Saintpaul with the same genetic fingerprint as the strain of bacteria that is causing the current outbreak in the United States.

As a result, until further notice, the FDA is advising consumers to avoid raw serrano peppers from Mexico, in addition to raw jalapeño peppers from Mexico, and any foods that contain them.

The test results announced today are part of the FDA's continuing intensive investigation into the outbreak of Salmonella Saintpaul. The investigation has involved tracing back, through complex distribution channels, the origins of products associated with clusters of illness in the United States, as well as inspections and evaluation of farms and facilities in this country and in Mexico, and the collection and testing of environmental and product samples. One of these tracebacks led to a packing facility in Mexico, and to a particular farm, where the agency obtained the samples.

Previously, FDA inspectors collected a positive sample of jalapeño pepper from a produce-distribution center owned by Agricola Zaragosa in McAllen, Texas. The FDA continues to work on pinpointing where and how in the supply chain this first positive jalapeño pepper sample became contaminated. It originated from a different farm in Mexico than the positive samples of serrano pepper and irrigation water.

The FDA is still analyzing many of the samples taken at various farms in Mexico. If laboratory results warrant, the FDA will provide consumers with additional cautions or warnings necessary to protect their health.

On July 17, the FDA announced it had determined that fresh tomatoes now available in the domestic market are not associated with the current outbreak. As a result, the agency removed its June 7 warning against eating certain types of red raw tomatoes.

Jack Distribution, LLC. Issues a Voluntary Nationwide Recall of all Lots of Rize 2 The Occasion Capsules and Rose 4 Her Capsules, Products Marketed as Dietary Supplements, Containing an Undeclared Ingredient

FOR IMMEDIATE RELEASE -- Pompano Beach, FL – July 28, 2008 – Jack Distribution, LLC, 1501 Green Road Unit C Pompano Beach, Florida 33064 and its wholesale distributors G & N works, Inc., and Devine Distribution, Inc., announced today that they are conducting a voluntary nationwide recall of all lot numbers of the company's supplement products sold under the brand names Rize 2 The Occasion and Rose 4 Her. New lots of Rize 2 and Rose 4 her (not subject to this recall) will contain lot numbers beginning in "BL".

Jack Distribution, LLC, is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Rize 2 and Rose 4 Her samples of random lots found the product contains potentially harmful, undeclared ingredients. FDA asserts that its chemical analysis revealed that Rize 2 The Occasion and Rose 4 Her contain thiomethisosildenafil, an analog of sildenafil, the active ingredient of a FDA-approved drug used for Erectile Dysfunction (ED). FDA maintains that this ingredient is close in structure to sildenafil and is expected to possess a similar pharmacological and adverse event profile. This undeclared chemical poses a potential threat to consumers because it may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.

Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

Customers who have this product in their possession should stop using it immediately and contact their physician if they have experienced any problems that may be related to taking this product.

Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.

The company advises that any unused portions can be returned to the place of purchase for a full refund of purchase price. Jack Distribution will manufacture new lots of these products which are not subject to the recall. Those lot numbers will begin with "BL" and will begin to be sold shortly.

Rize 2 and Rose 4 Her are sold in adult stores, vitamin & nutrition shops, convenience stores, and via the internet nationwide. The Rize 2 product is sold as a (single blister pack, three count bottles, twelve count bottles, and thirty count bottles. Rose 4 Her is only available in single blister packs and three count bottles.

The Company is taking this voluntary action because it is committed and is always concerned with the health of persons who have consumed this product. The Company is reviewing the procedures and policies of all firms involved with the manufacture of the product to ensure that there will be no future issues with regard to Rize 2 and Rose 4 Her pills composition. The Company is working closely with the FDA in the recall process and is committed to the quality and integrity of its products. It sincerely regrets any inconvenience to consumers and its other customers.

Publix Issues Recall for No Sugar Added Cherry Pie

FOR IMMEDIATE RELEASE -- LAKELAND, FL -- July 24, 2008 -- Publix Super Markets is issuing a voluntary recall on three codes of No Sugar Added Cherry Pie with a sell-by-date of July 8 – July 27. UPC numbers for the affected product may be found on the back label below the Nutritional Facts panel:

• Publix NSA 8inch Cherry Pie, UPC: 41415-65990
• Publix NSA 1/2 Cherry Pie, UPC: 03000-00225
• Publix NSA 1/4 Cherry Pie, UPC: 41415-66990

These products were sold in the retail bakeries and were recalled due to the undeclared soy ingredient. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products. The recall affected stores in Georgia, Alabama, South Carolina, Tennessee and Florida stores in Citrus County south through Monroe County, excluding Orlando proper stores.

"The packaging error was detected during a routine label review," said Maria Brous, Publix media and community relations director. "As part of our commitment to food safety, we routinely inspect our product labeling for accuracy and for product quality. There have been no reported cases of illness. Customers who have purchased the product may return it to their store for a full refund or replacement. Consumers with questions may contact Publix at 1-800-242-1227."

NOTE: "According to the Texas and North Carolina Departments of Health, the strain of Salmonella found in this company's jalapeño and serrano peppers and in its avocado is not Salmonella Saintpaul, and is not believed to be related to the current Salmonella outbreak.

The recall is a result of sampling not by the U.S. Food and Drug Administration (FDA) but by the Texas Department of State Health Services (Texas Health) and the North Carolina Department of Health and Human Services (North Carolina Health ) which revealed that these products contained the bacteria.

The company has voluntarily initiated a recall of its already distributed products and has stopped future distribution while the FDA, Texas Health, North Carolina Health and the company continue to investigate to determine the source of the problem."
 

Grande Produce, LTD.CO Recalls Jalapeno Peppers, Serrano Peppers, and Avocados Because of Possible Health Risk

FOR IMMEDIATE RELEASE -- July 19, 2008 -- Grande Produce, LTD. CO of Hidalgo, Texas (hereinafter referred to as Grande Produce) is recalling Jalepeno Peppers and Serrano Peppers distributed between May 17th and July 17th, 2008; and Avocados, all sizes, with lot #HUE08160090889 because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The Jalapeno Peppers, Serrano Peppers and Avocados were distributed to the following states: TX, DE, NC, GA, OK, IA, MN, IL, FL, IN, MD, NY, MS, AR, KS, and KY.

The avocados being recalled were shipped in boxes labeled "Frutas Finas de Tancitaro HASS Avocados, Produce of Mexico," all sizes, with lot number HUE08160090889. The Jalapeno Peppers and Serrano peppers being recalled were shipped in 35lb. plastic crates with no brand name or label.

No illnesses associated with this recall have been reported to date.

The recall is a result of sampling by the Texas Department of State Health Services and The North Carolina Department of Health and Human Services, which revealed that these products contained the bacteria. Distribution of these products has been suspended while FDA, the Texas Department of State Health Services, The North Carolina Department of Health and Human Services and the company continue their investigation as to the source of the problem.

Consumers who purchased Avocados, Jalapeno Peppers and Serrano Peppers should contact their supplier to determine if their products are involved in the recall. Consumers with questions may contact the company at (956) 843-8575.

Roxane Laboratories, Inc. Initiates a Nationwide Voluntary Recall of Two Manufacturing Lots of Sodium Polystyrene Sulfonate Suspension in the US and Puerto Rico

FOR IMMEDIATE RELEASE -- Columbus, Ohio -- July 14, 2008 -- Roxane Laboratories, Inc. announced today that it is conducting a nationwide voluntary recall of two manufacturing lots of Sodium Polystyrene Sulfonate Suspension, USP, 15 g/60 mL Unit dose bottles (NDC 0054-0165-51; Lot 856396A Exp April 2010, and Lot 856693A Exp May 2010). Sodium Polystyrene Sulfonate Suspension is used to treat hyperkalemia (an elevated blood level of the electrolyte potassium).

Roxane Laboratories' number one priority is for the safety of patients who use our products. A sample from product lot 856396A tested positive for a strain of yeast, which could potentially affect immunocompromised patients. Roxane Laboratories believes that this may be attributed to yeast contamination in one lot of high-density polyethylene bottles received from a supplier. There are various manifestations of yeast infections. The risk of developing a yeast infection depends on how immunocompromised the patient is. Additionally, there are a range of symptoms in a yeast infection from thrush, skin rash, and blood infections (sepsis). If patients develop an infection they should consult their physician. Due to the potential risks that could occur in immunocompromised patients, Roxane Laboratories is voluntarily recalling lot 856396A. Although there have been no testing failures associated with lot 856693A, this additional lot is also being included in the recall as a precautionary measure because the same lot of bottles was used in both finished product lots. All other product parameters were within specification and product efficacy is not impacted. There have been no complaints or adverse events reported for the affected lots. This recall is limited to the two lot numbers listed. No other Roxane Laboratories, Inc. products or lots are impacted by this recall.

Information has been sent to Pharmacists alerting them of the details pertaining to this recall. As described in these recall communications, pharmacists who may have dispensed Sodium Polystyrene Sulfonate Suspension, USP, 15 g/60 mL Unit dose bottles from Lots 856396A and 856693A are instructed to contact those patients to return the affected product to the pharmacist.

Pharmacists and wholesalers that have any Sodium Polystyrene Sulfonate Suspension, USP, 15 g/60 mL Unit dose bottles from Lot 856396A or Lot 856693A have been instructed to discontinue distribution and use of these lots immediately and contact Capital Returns at 888.839.7837 for any questions regarding the recall returns. Requests for additional information should be referred to Roxane Laboratories Technical Product Information at 800.962.8364.

Advice For Patients Taking Sodium Polystyrene Sulfonate Suspension USP, 15 g/60 Ml Unit Dose Bottles

If your pharmacist has notified you that you may have received a bottle from one of the lots listed in this recall, please return your Sodium Polystyrene Sulfonate Suspension, USP, 15 g/60 mL Unit dose bottles to your pharmacist.

If you have NOT been notified by your pharmacist, please check your product to determine if it is from either of the two affected lots: Sodium Polystyrene Sulfonate Suspension, USP, 15 g/60 mL Unit dose bottles from Lot 856396A Exp April 2010, or Lot 856693A Exp May 2010. If the product has either of these two lot numbers on the bottle, please contact your pharmacist for further instructions. This recall has been limited to these two specific lots.

Roxane Laboratories is working with the US FDA on this voluntary recall. The products discussed in this press release are available by prescription only, and no injuries have been reported in relation to this issue.

Lucky Green Trading, Inc. Recalls Thai Basil Because of Possible Health Risk

FOR IMMEDIATE RELEASE -- Garden Grove, CA -- July 9, 2008 --- LUCKY GREEN TRADING, INC. of Garden Grove, CA is recalling Thai Basil , because it has the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

Thai Basil was distributed through retail stores and direct delivery to customers in Southern California, Arizona , and Nevada on June 30, 2008.

The product was shipped in 14 LB cardboard cartons with 12 individual packages weighting approx.1.2 LB each in clear, unmarked, plastic bags. The exterior cartons were labeled "16 DE SEPTIEMBRE S/N SANTA ROSA TAPACHULA NAYARIT, C.P. 63731" "Thai Basil" and also had an attached sticker with Airway Bill #027 1947 0861.

No illnesses have been reported to date.

The recall was as the result of a random testing by the FDA which revealed that the finished products contained the Salmonella . The company has suspended distribution and importation of the product as FDA and the company continues their investigation.

Consumers who purchased basil should contact the store where they purchased the product to determine if their basil is the Thai basil involved in the recall. Consumers with questions may contact the company at (714) 554-9293.

Giant Food Alerts Customers to Voluntary Recall of Giant Brand Garlic Bread and Garlic Spread

FOR IMMEDIATE RELEASE -- June 27, 2008 - Landover, MD -- Giant Food has announced a voluntary recall of Giant brand garlic bread and garlic spread products sold in its Bakeshop as the items contain milk products which are not declared on the labels. Giant removed from its shelves all 16 ounce packages of Giant brand garlic bread and all 16 ounce packages of Giant brand garlic spread products.  

The following products are affected by this recall:

• 16 oz. Giant Garlic Bread: UPC #21476670000

• 16 oz. Giant Garlic Spread: UPC #20173310000

People who have an allergy or severe sensitivity to dairy products run the risk of serious or life-threatening allergic reaction if they consume these products.  No illnesses have been reported.

Customers who have purchased the affected products may return them to Giant for a full refund. Customers looking for additional information may call Giant Customer Service at (888) 469-4426 for more information. Customers can also visit the Giant website at www.giantfood.com.

Stop & Shop Alerts Customers to Voluntary Recall of Stop & Shop Brand Garlic Bread and Garlic Spread

FOR IMMEDIATE RELEASE -- June 27, 2008 – Quincy, MA -- The Stop & Shop Supermarket Company has announced a voluntary recall of Stop & Shop brand garlic bread and garlic spread products sold in its Bakeshop as the items contain milk products which are not declared on the labels. Stop & Shop removed from its shelves all 16 ounce and 9 ounce packages of Stop & Shop brand garlic bread and all 16 ounce packages of Stop & Shop brand garlic spread products.  

The following products are affected by this recall:

• 16 oz. Stop & Shop Garlic Bread: UPC #20540880000

• 9 oz. Stop & Shop Garlic Bread: UPC #20540900000

• 16 oz. Stop & Shop Garlic Spread: UPC #20549280000

People who have an allergy or severe sensitivity to dairy products run the risk of serious or life-threatening allergic reaction if they consume these products.  No illnesses have been reported.

Customers who have purchased the affected products may return them to Stop & Shop for a full refund or call Stop & Shop Customer Service at (800) 767-7772 Monday through Friday from 9 a.m. to 5 p.m. for more information. Customers can also visit the Stop & Shop website at www.stopandshop.com.

FOR IMMEDIATE RELEASE -- June 18, 2008, Boise, ID – Matterhorn Group Inc is recalling certain date coded product of their Rainbow Glacier "Astro Pops" water ice frozen novelty pops, Cherry Pineapple Swirl 3.5 oz size 12 count bag pack, with tag closure "Best by JUN 03-09", "Best by JUN 04-09" and "Best by JUN 05-09" sold through the Wal-Mart stores located in California and Arizona, Sunnyside Farms "Missile Pops" Cherry Pineapple in 3.5 oz. size 12 count bag packages, with tag closure of "Best By JUN 02-09", "Best by JUN 03-09", and "Best by JUN 04-09" sold through the California stores of grocery retailers Save Mart and Raley’s, and Vitafreze Frozen Astronot Pops 3.5 oz size 12 count bag packages, with tag closure of "Best By JUN 02-09" sold in California. The products are being recalled because they may contain pieces of hard plastic. Only the noted product date codes listed are affected.

The small pieces of non-toxic hard plastic were from a part of the processing equipment which broke during the manufacturing process. The majority of the possibly affected product was retrieved from the distribution system before any release to retail stores. However, there were a small number of cases which were shipped to above mentioned locations.

There have been no reports of injury. People who bite into or swallow a fragment could possibly be injured, prompting this precautionary recall. Young children are particularly at risk of a choking hazard. Although the company believes the problem is very isolated, we are taking this measure to ensure the safety of our consumers.

Consumers in AZ and CA who have purchased the above indicated products should return them to their retailer where purchased for a full refund. For questions and inquiries, consumers may contact us at 1-888-264-0898.

FOR IMMEDIATE RELEASE -- (GREENWICH, Connecticut, June 24, 2008) – This announces a product recall for the one-gallon Nestlé Pure Life Purified Drinking Water sold ONLY in Shop-Rite stores in the five Northeast states of Connecticut, Delaware, New Jersey, New York and Pennsylvania. This affects ONLY the one-gallon size.

Fewer than 150 one-gallon bottles of Nestlé Pure Life Purified Water are implicated, produced in a short timeframe on May 5, 2008 between 8:00 AM and 9:00 AM. The product date code is printed on the shoulder of one-gallon bottles. The code is:

First line…………050508126WF024
Second line……... Starts with the numbers "08"
For example: 0801BB05/2010

The product in question may contain a diluted form of a common food grade cleaning compound that results in a bitter or sour taste. This could pose a potential health concern if ingested in large quantities over an extended period of time and should not be consumed or used in preparing infant formulas or other foods or beverages. No illnesses have been reported.

To further assure consumers, Shop-Rite, as of Monday, June 23rd, has removed any remaining affected product from their stores and warehouses.

Consumers who possess this product or have questions should contact the company at a toll free number 866-599-8980 available 24 hours a day. This same toll-free number is also printed on the front of all product labels for the one-gallon size.

FOR IMMEDIATE RELEASE -- June 23, 2008 -- Fresca Italia of Brisbane, CA is recalling Burrata, a type of cheese, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as fever, headache, stiffness, nausea, abdominal, or diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

This product was distributed in the San Francisco Bay Area and Southern California in retail stores and restaurants.

This product weighs approximately 8.8oz and is packaged in a white and green plastic wrapper with the manufacturer’s name, "Caseificio Voglie di Latte" and the product name "Burrata." ALL LOT CODES AND EXPIRATION DATES from this manufacturer are subject to recall. Previously, the only batch subject to the recall will be labeled with the expiration date of 24/5/2008. The following quantities were distributed:

606 lbs with the Lot Code 24/5/2008

661 lbs with the Lot Code 31/5/2008

490 lbs with the Lot Code 07/06/2008

The recall is the result of survey sampling by the California Dept. of Food & Agriculture which revealed that the product in question contained the bacteria. Fresca Italia has immediately halted further distribution. This recall is an expansion of the previous recall initiated on May 30, 2008. Positive results for Listeria were found in other lots of the product by the Food and Drug Administration.

If you have any Caseificio Voglie di Latte Burrata with an expiration of 24/5/2008 please return it to the place of purchase for a full refund. Consumers with questions may contact the company at 415-468-9800.

Lake Country® and LAND O LAKES® Lamb Feed Voluntary Recall
Elevated Levels of Copper Found

FOR IMMEDIATE RELEASE -- (St. Paul, Minn.) June 11, 2008 – The Land O’Lakes Purina Feed plant in Fremont, Neb., has initiated a limited voluntary recall of four lamb feed products, packaged in 50-pound bags, due to the potential for higher than acceptable levels of copper.

The products and lot numbers involved in the recall were produced at the Fremont, Neb., feed plant only, and are described as:

Lot numbers range from Jan. 1, 2008, to May 30, 2008, and are listed on the bag as 8JAN01FRE1 to 8MAY30FRE1 inclusive.

On bagged products, the lot numbers are printed on both the tag and sewing strip of each bag. Lot numbers are formatted as follows: Example 8MAY30FRE1 – 8=Year / MAY= Month / 30=Day of Month / FRE1=Plant Code.

The first two products included in this recall (Honor Lamb Show Grower DX Pellet and Honor Lamb Show Grower Starter DX Pellet) were previously announced in a June 6, 2008, news release and retailer contacts – and were distributed only in the following areas: Nebraska, north central Kansas, northwest Colorado, southern Minnesota, and western and south central Iowa.

The latter two products (Honor Show Lamb Grower B30 Pellet and Lamb Grower-Finisher B30) were distributed only in eastern Nebraska, northeast Kansas and western Iowa.

The recall was initiated after receiving a customer complaint regarding lamb mortalities. The presence of copper above acceptable levels can cause serious health issues, and at high levels, mortality in sheep.

Retailers have been contacted to quarantine these products and notify customers who purchased the product. The affected product should not continue to be stored or used. Customers who purchased these products will receive replacement product.

For more information on the product recall, contact Customer Service at 1-877-585-2365.

ETHEX Corporation Voluntarily Recalls a Single Lot of Morphine Sulfate 60 mg Extended Release Tablets Due to the Potential for Oversized Tablets

FOR IMMEDIATE RELEASE -- St. Louis, MO – June 9, 2008 – ETHEX Corporation announced today that it has voluntarily recalled a single lot of morphine sulfate 60 mg extended release tablets (Lot No. 91762) due to a report of a tablet with twice the appropriate thickness. Oversized tablets may contain as much as two times the labeled level of active morphine sulfate. The lot was distributed by ETHEX Corporation under an "ETHEX" label between April 16th and April 27th of 2008. No other dosage strength, nor any other lot of the 60 mg strength is affected by this recall.

The voluntary single-lot recall is due to a report that a tablet with as much as double the appropriate thickness was identified and the possibility therefore that there may be other similar oversized tablets that may have been commercially released in the affected lot. Such tablets may contain as much as twice the labeled level of active morphine ingredient. The product is a white oval tablet with "60" on one side, and "E" on the reverse.

No report of unexpected side effects or injury has been received. However, opioids such as morphine have life-threatening consequences if overdosed. Those consequences can include respiratory depression (difficulty or lack of breathing), and low blood pressure. Many patients for whom this product is prescribed are likely to be highly debilitated with reduced strength or energy as a result of illness. As such, they may be less likely to be able to determine that a tablet is overweight or oversized than an unimpaired individual.

Any customer inquiries related to this action should be addressed to ETHEX Customer Service at 1-800-321-1705, or fax to ETHEX Customer Service at 314-646-3751 or sent via email to: customer-service@ethex.com with representatives available Monday through Friday, 8 am to 5 pm CST.

ETHEX Corporation previously initiated the recall notification to wholesalers and retailers who have received any inventory of the recalled lot of this product with instructions for returning the recalled product and, if they have not already done so, they are urged to contact the number above regarding procedures for returning the recalled product. If consumers have any questions about the recall, they should call the number above, their physician, their pharmacist or other health care provider.

This recall is being conducted with the knowledge of the Food and Drug Administration (FDA).
Any adverse reactions experienced with the use of this product, and/or quality problems may also be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch.

International Pharmaceuticals, Ltd. Issues a Voluntary Recall of all Viril-Ity-Power (VIP) Tabs, a Product Marketed as a Dietary Supplement

FOR IMMEDIATE RELEASE -- Bradford, MA - May 29, 2008 - International Pharmaceuticals, Ltd., P.O. Box 5165, Bradford, MA 01835, announced today that it is conducting a voluntary recall of all the company’s supplement product sold under the brand name of Viril-Ity-Power (VIP) Tabs, 560mg/serving.

International Pharmaceuticals, Ltd. is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of a sample from one lot of the product revealed that it contained a potentially harmful undeclared ingredient, hydroxyhomosildenafil.  FDA asserts that this ingredient is an analog of sildenafil.  Sildenafil is the active chemical ingredient of an FDA-approved drug used for Erectile Dysfunction (ED) in men to enhance sexual performance. The use of undeclared chemicals pose a threat to consumers because they may harmfully interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.  Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take such nitrates.

VIP Tabs are sold in retail outlets nationwide and are packaged into 2-capsule blister packs and 8-capsule bottles.

Customers who have this product in their possession should stop using it immediately and contact their physician if they have experienced any problems that may be related to taking this product. 

The Company advises that any unused portions be returned to CB Distributors in Benoit, Wisconsin, in accordance with return instructions/questions obtained by calling (800)-273-4137, Ext. 3.

Any adverse events that may be related to the use of this product should be reported to the FDA’s MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or online at www.fda.gov/medwatch/report.htm.

The Company is working closely with the FDA in the recall process and is taking this voluntary action because it is committed to the quality and integrity of it’s products, and is always concerned with the health of persons who may have consumed this product. 

The Company sincerely regrets any inconvenience to consumers, and is reviewing the procedures and policies of all firms involved with the manufacture of this product to ensure that there will be no subsequent issues with regard to the composition of this product in the future. 

Lifetime Brands Voluntarily Recalls Certain Items Nationwide from its Pfaltzgraff® Villa della Luna® pattern and Nautica J Class® pattern (Red Only) Stoneware Dinnerware Product Lines

Contact:
(800) 499-1976 – For Pfaltzgraff® Dinnerware
(866) 928-0060 – For Nautica® Dinnerware

FOR IMMEDIATE RELEASE -- April 28, 2008 -- Lifetime Brands, Inc., of Garden City, New York, today announced that, as a result of its internal compliance and independent product testing programs, it recently became aware that certain Pfaltzgraff® Villa della Luna® pattern and Nautica J Class® pattern stoneware dinnerware products may exceed the Food and Drug Administration’s (“FDA”) guidance levels for lead and/or cadmium.  No illness related to these products has been reported to date.
Specifically, the following products are subject to this recall:

These dinnerware products may have been sold as part of a set or individually online and through retail stores nationwide.

For additional information regarding the recall, please contact us by dialing the following toll free numbers:
(800) 499-1976 – For Pfaltzgraff® Dinnerware
(866) 928-0060 – For Nautica® Dinnerware

Fine Land Corp Issues Alert on Undeclared Sulfites in Ying Feng Foodstuffs Brand Dried Bulbus Lily

FOR IMMEDIATE RELEASE -- Brooklyn, NY -- April 11, 2008 --- Fine Land Corp, 239 Bay 20th Street Brooklyn NY 11214, is recalling its Ying Feng Foodstuffs brand Dried Bulbus Lily because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

The recalled Ying Feng Foodstuffs brand Dried Bulbus Lily comes in a 10 ounce uncoded clear plastic package.  The product was sold nationwide. It is a product of China.

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in Ying Feng Foodstuffs brand Dried Bulbus Lily which did not declare sulfites on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.

No illnesses have been reported to date. Consumers who have purchased packages of Ying Feng Foodstuffs brand Dried Bulbus Lily are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 917-939-5595.

FOR IMMEDIATE RELEASE --Brooklyn, NY -- April 8, 2008 --- Fine Land Corp, 239 Bay 20th Street Brooklyn NY 11214, is recalling its Ying Feng Foodstuffs brand dried snow fungus because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

The recalled Ying Feng Foodstuffs brand dried snow fungus comes in a 3 ounce uncoded clear plastic package.  The product was sold nationwide. It is a product of China.

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in Ying Feng Foodstuffs brand dried snow fungus which did not declare sulfites the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.

No illnesses have been reported to date. Consumers who have purchased packages of Ying Feng Foodstuffs brand dried sow fungus are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 718-714-1850.

FOR IMMEDIATE RELEASE -- Harrisburg, PA -- April 7, 2008 -- Consumers who purchased raw milk from Piney Ridge dairy farm in New Bethlehem, Clarion County, and Clark and Elaine Duncan’s farm in Meadville, Crawford County, anytime after March 10 should discard it immediately due to the risk of Listeria Monocytogenes contamination, Agriculture Secretary Dennis Wolff said today.

Raw milk is milk that has not been pasteurized or homogenized. Pennsylvania farms selling raw milk must be permitted and inspected to reduce health risks associated with the unpasteurized products. In 2007, a previous case of Listeria Monocytogenes was found at Piney Ridge dairy.

"During routine testing, samples taken at the dairies tested positive for Listeria Monocytogenes," said Wolff. "If consumers have raw milk from these farms, they should discard it immediately."

No illnesses have been reported as a result of the potential contamination, but if people who consumed the raw milk become ill, they should consult their physicians.

The Department of Agriculture has suspended sales of raw milk at the dairies and is requiring corrective action be taken. Samples were taken from the farms on March 31; they tested positive for Listeria Monocytogenes on April 4.

Multiple laboratory samples must test negative before sales can resume.

Symptoms of Listeriosis are fever, muscle aches, and sometimes gastrointestinal symptoms such as nausea or diarrhea. If infection spreads to the nervous system, symptoms such as headache, stiff neck, confusion, loss of balance or convulsions can occur.

Infected pregnant women may experience only a mild, flu-like illness, but infections during pregnancy can lead to miscarriage or stillbirth.

Symptoms of Listeriosis can appear in four days to three weeks.

FOR IMMEDIATE RELEASE -- April 1, 2008 -- Grand Supercenter, Inc. of Lyndhurst, NJ is recalling the following product because they have the potential to be contaminated with Clostridium botulinum, a bacterium, which can cause life-threatening illness or death.

HC Fresh, Frozen Salted Croaker,
Net. Wt.: 16.9 oz (480 gram),
Item # HC 0500402,
Expiration Date: Aug 02. 2009

Consumers are warned not to use these products even if they do not look or smell spoiled.

Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision, and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.

HC Fresh Frozen Salted Croaker was distributed through H Mart stores including H Mart and Super H Mart in New York, New Jersey, Pennsylvania, Illinois and Texas area.

The potential for contamination was noted after routine inspection. No illnesses have been reported to date in connection with this problem.

Consumers who have purchased these HC Fresh Frozen Salted Croaker products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Grand Supercenter, Inc. at 201-507-9900.

FOR IMMEDIATE RELEASE -- Fort Worth, Texas -- April 1, 2008 -- Mrs Baird's Bakeries announced today that it has voluntarily recalled packages of 4 inch buns because the product contains milk that is not listed on the label.

Individuals with allergies to milk run the risk of a serious or life threatening reaction if they consume this product. No illness or allergic reactions have been reported. No other products are involved in this voluntary recall.

The buns were sold at Costco stores in North Texas in a two count package containing 24 buns and to restaurant and institutional customers in Texas and Oklahoma in 12 count packages. The package label reads:

Mrs Baird's
Enriched
12 Buns
NET WT 21 OZ (1LB 5 OZ) 595g
With a Best by date of April 8, 2008.

The problem was discovered during routine operations at the plant by an employee monitoring the use of packaging.

Consumers can return the product to their place of purchase for a full refund or exchange. Consumers with questions may contact Mrs Baird's at (877) 224-7374.

The quality of our products and safety of our consumers is our foremost concern. The company will continue to work with the retailers to resolve this issue as quickly as possible. The FDA has been advised of this action.

FOR IMMEDIATE RELEASE -- MANSFIELD, Massachusetts – March 28, 2008 - Covidien, formerly Tyco Healthcare, was recently notified by its supplier, Scientific Protein Laboratories LLC (SPL), of a nation-wide recall of Heparin Sodium USP active pharmaceutical ingredient. The voluntary recall affects the following 32 lots manufactured and distributed by Covidien in the United States.

Covidien began recalling the lots today as a precautionary measure. This product recall was initiated due to a notification received from the supplier, SPL, disclosing that two lots of Heparin Sodium USP Active Pharmaceutical Ingredient acquired by Covidien had a heparin-like contaminant. To date, Covidien has not received any adverse event reports related to this issue. Although a very small product line for Covidien, the Company is committed to following the direction of the Food and Drug Administration (FDA) regarding this matter.

The FDA has received reports of serious injuries and/or deaths in patients who have been administered Heparin injectable products of other companies containing this contaminant. As indicated in the notification issued by the supplier SPL, typical symptoms include anaphylactic-like reactions such as low blood pressure, shortness of breath, nausea, vomiting, diarrhea and abdominal pain.

Adverse reactions or quality problems experienced in the U.S. with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Online: www.fda.gov/medwatch/report.htm

Regular Mail: use postage-paid FDA form 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to: MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787

Fax: 1-800-FDA-0178

Customers who have product in their possession from the recalled product lots should discontinue use immediately. Patients reporting any problems that may be related to the use of this product should be advised to contact a physician. Customers with questions about the return of recalled product should contact the Return Coordinator at 1-800-346-7197, ext. 8677, between 8:30am – 5:00pm (ET), Monday through Friday.

Consumers who have purchased these products are urged to return them to the place of purchase. Customers with questions may contact Luis Alvarado of Tropifresh, Inc. at 213-745-81111.

Voluntary Recall on Honduran Cantaloupes Due to Potential Health Concerns

FOR IMMEDIATE RELEASE -- Westlake Village, Calif., March 28, 2008 -- Dole Fresh Fruit Company, a subsidiary of Dole Food Company, Inc., has voluntarily recalled all Honduran Cantaloupes grown, packed and shipped by an independent third-party grower, Agropecuaria Montelibano of San Lorenzo Valle, Honduras.

This recall has been initiated based on current information from the U.S. Food and Drug Administration that fruit from this company appears to be associated with a Salmonella Litchfield outbreak in the United States and Canada.

Persons infected with Salmonella may experience a variety of symptoms and illnesses. According to the U.S. Food and Drug Administration, healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in more severe illnesses and potentially can be fatal.

The cantaloupes were distributed for sale throughout the United States and parts of Canada in cardboard cartons with the brand "Dole" and "PRODUCT OF HONDURAS" printed on each of the side panels of the carton.

Publix Issues Recall for Assorted Flavors of Empanadas

FOR IMMEDIATE RELEASE -- Lakeland, FL -- March 14, 2008 -- Publix Super Markets is issuing a voluntary recall on all codes of prepackaged 2 and 4-pack Apple, Pineapple and Pumpkin Empanadas sold in retail bakeries due to the undeclared milk ingredient. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. The recall affects the following 10 counties:

• Clayton, Ga.
• Cobb, Ga.
• Collier, Fla.
• DeKalb, Ga.
• Davidson, Tn.
• Fulton, Ga.
• Gwinett, Ga.
• Hall, Ga.
• Houston, Ga.
• Lee, Fla.

The product was sold in a variety of different containers.

"The packaging error was detected during a routine label review," said Maria Brous, Publix media and community relations director. “As part of our commitment to food safety, we routinely inspect our product labeling for accuracy and for product quality. There have been no reported cases of illness. Customers who have purchased the product may return it to their store for a full refund or replacement. Consumers with questions may contact Publix at 1-800-242-1227."

-- Cleveland, OH -- February 20, 2008 -- Pierre’s Ice Cream Company, in cooperation with the Food and Drug Administration, is voluntarily recalling its Pierre’s Homestyle Dutch Chocolate Ice Cream (purple 56 fl oz package) because it may contain undeclared peanut butter cup candies. The containers are identified with the code 07320 which is printed on the rim of the lid.

People who have an allergy or severe sensitivity to peanuts run the risk of developing a life threatening health problem/illness if they consume this batch of Dutch Chocolate. No illnesses have been reported to date.

This ice cream was distributed in Ohio, Michigan, Western Pennsylvania, and Indiana and reached consumers through retail stores. The packaging does not reveal the presence of peanut butter candy or peanuts on the ingredient label.

If consumers have a Dutch Chocolate 56 fl oz (purple package) with the code 07320 on the rim of the lid, they should discard the ice cream and send the lid of the empty container back to Pierre’s for a full refund:

Consumer Response Department
Pierre’s Homestyle Dutch Chocolate Refund
6200 Euclid Ave
Cleveland, OH 44103
For any questions, consumers are asked to call 1-216-432-1144

FOR IMMEDIATE RELEASE -- February 15, 2008 -- Nutri-Foods, Inc. ("Nutri-Foods") of Royal Oak, Michigan, is recalling its .50 pound packages of "Organic Sesame Seeds Natural - Unhulled" due to possible salmonella contamination, an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illness such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The recalled "Organic Sesame Seeds Natural - Unhulled" were sold at Nutri-Foods.

The product comes in a .50 pound clear plastic package with a product SKU #170 at the top and a "packed on" date of December 28. This product was sold from circa December 15, 2007 through January 28, 2008.

No illnesses have been reported to date in connection with this problem.

Production of the product has been suspended while the FDA and manufacturer of the product continue their investigation.

Consumers who have purchased the .50 pound package are urged to return them to Nutri-Foods for a full refund. Consumers with questions may call Nutri-Foods at (248) 541-6820 and ask for John B. or Judy.

FOR IMMEDIATE RELEASE -- February 11, 2008 -- Rocky Mountain Popcorn Company, Centennial, CO is voluntarily initiating a nationwide recall of 1,603 bags of Low Fat Caramel 9 oz. Popcorn (in the green bag). This recall is on the Low Fat variety only. An ingredient in this product has been found to contain a trace amount of tree nuts, which potentially could cause an allergic reaction to any person with a tree nut allergy.

Consumers who have tree nut allergies and have purchased Rocky Mountain Popcorn’s Low Fat Caramel 9 oz. Popcorn (in the green bag) which is being recalled should stop using this item and contact Rocky Mountain Popcorn Company for a refund.

The recall includes only one flavor of the company’s ready to eat popcorn and it is Low Fat Caramel 9 oz. Popcorn (in the green bag). UPC #10449 32050 – with a manufacturing code less than D1231xx.

The company has voluntarily recalled the product after learning that the supplier of one of the ingredients in the formulation of Low Fat Caramel 9 oz. Popcorn (in the green bag) had changed its formulation to contain trace amounts of tree nuts. FDA has been apprised of this action.

The company has acquired an ingredient to replace the suspect ingredient that does not contain tree nuts, therefore future manufacturing of this product will not contain tree nuts. Again, only Low Fat Caramel with a manufacturing code less than D1231xx is affected by this recall.

No allergic reactions have been reported. Furthermore, there has been very limited distribution of this item, and it has been mostly in the Denver, CO area. All future sales of this item will be packaged in clearly and correctly labeled bags.

Low Fat Caramel 9 oz. Popcorn (in the green bag) was distributed to Colorado grocery and Convenience stores, only 100 units were distributed outside of the state of Colorado, in Ft. Worth, Texas. The product can be identified by a silver bag with green graphics.

Rocky Mountain Popcorn Company is notifying its distributors and customers by phone, email and letter, and is arranging for refund of this item to customers who have uneaten bags of popcorn, and who suffer from tree nut allergies.

Customers should contact Rocky Mountain Popcorn Company directly at 303.744.8850 or by email at info@rmpopcorn.com , and provide proof of purchase (a receipt and UPC code) for unused product reimbursement of Low Fat Caramel 9 oz. Popcorn (in the green bag).

Consumers with questions may contact Rocky Mountain Popcorn @1.888.744.8850.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, or by regular mail or by fax.

Online: www.fda.gov/medwatch/report.htm’
Regular Mail: MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787
Fax: 1-800-FDA-0178

FOR IMMEDIATE RELEASE -- Oakland, CA -- January 22, 2008 -- Dreyer's Grand Ice Cream is voluntarily recalling 90 cartons of Dreyer's Slow Churned® Light Caramel Delight ice cream and Slow Churned Light Butter Pecan ice cream distributed in Colorado, Idaho, Oregon and Wyoming, because the ice cream may contain pecans not identified on the label.

The potentially affected cartons are the 1.75-quart size of Dreyer's Slow Churned Light Caramel Delight and Slow Churned Light Butter Pecan ice cream. The sides of the Slow Churned Light cartons identify the flavor as Caramel Delight, but the carton lids identify it as Butter Pecan. The actual flavor of the ice cream may be Butter Pecan erroneously packaged in Caramel Delightcartons, so Dreyer's is recalling the ice cream to avoid any confusion among consumers who may be allergic to pecans.

Less than 90 mislabeled cartons are believed to be in the marketplace. These products are sold in various retail grocery stores. The affected cartons have the following specific code printed on the bottom of the carton:

BEST IF PURCHASED BY 09/11/08
049-32

No other Dreyer's ice cream products or codes are affected.

Individuals who have an allergy or severe sensitivity to pecans may run the risk of serious or potentially life-threatening allergic reaction if they consume this product. People with a pecan allergy or sensitivity should not consume the ice cream and should immediately dispose of the product.

No consumers have reported symptoms of allergic reaction. Dreyer's Grand Ice Cream is working with the U.S. Food and Drug Administration in implementing this voluntary product recall and is investigating the incident. Dreyer's is also working with the Food Allergy and Anaphylaxis Network to alert consumers in the four states.

Consumers who have purchased the ice cream with this code should call the Dreyer's Consumer Call Center at 1 888 837-4438, for a full refund. Dreyer's Grand Ice Cream manufactures and distributes ice cream and frozen snacks across the United States.

FOR IMMEDIATE RELEASE -- Raritan, NJ – February 12, 2008 – PriCara, Division of Ortho-McNeil-Janssen Pharmaceuticals, Inc. said today that all lots of 25 microgram/hour (mcg/hr) DURAGESIC® (fentanyl transdermal system) CII patches sold by PriCara in the United States and all 25 mcg/hr fentanyl patches sold by Sandoz Inc. in the United States are being voluntarily recalled as a precaution from wholesalers and pharmacies. The recalled patches all have expiration dates on or before December 2009, and all are manufactured by ALZA Corporation, an affiliate of PriCara. The recall is being conducted in cooperation with the U.S. Food and Drug Administration. All 25 mcg/hr fentanyl patches manufactured by ALZA and sold in Canada also are being recalled.

DURAGESIC 25 mcg/hr (fentanyl transdermal system) and Sandoz Inc. 25 mcg/hr fentanyl transdermal system patches being recalled may have a cut along one side of the drug reservoir within the patch. The result is possible release of fentanyl gel from the gel reservoir into the pouch in which the patch is packaged, exposing patients or caregivers directly to fentanyl gel. As per the approved product labeling for DURAGESIC, fentanyl is a potent Schedule II opioid medication. Fentanyl patches that are cut or damaged in any way should not be used. Exposure to fentanyl gel may lead to serious adverse events, including respiratory depression and possible overdose, which may be fatal. Anyone who comes in contact with fentanyl gel should thoroughly rinse exposed skin with large amounts of water only; do not use soap. Immediately dispose of affected patches with cut edges by flushing them down the toilet, using caution not to handle them directly. Patches with a cut edge that have leaked gel will not provide effective pain relief.

Anyone who has 25 mcg/hr DURAGESIC or Sandoz Inc. fentanyl patches should check the box or foil pouch for the expiration date to see if they have patches that are being recalled. The recalled patches all have expiration dates on or before December 2009. The cut edge in affected patches can be seen upon opening the sealed foil pouch that holds the patch. Affected patches should not be handled directly.

Anyone with 25 mcg/hr Sandoz Inc. patches being recalled should call 800-901-7236.

Patients using fentanyl patches who have medical questions should contact their health-care providers.

For more information, visit www.DURAGESIC. com.

DURAGESIC is used to manage persistent moderate to severe chronic pain that needs to be treated around the clock and which cannot be treated by: combination narcotic, short-acting, or non-narcotic pain treatment products. It should only be used by people who are receiving or have developed a tolerance to pain therapy with opioids. DURAGESIC should not be used if patients have pain that will go away in a few days, such as pain from surgery, medical or dental procedures, or short-lasting conditions. Any adverse reactions experienced with the use of fentanyl patches should be reported to the appropriate company using the telephone numbers above. DURAGESIC brand and other fentanyl patches are available by prescription only, through pharmacies, and should be used only under the supervision of a physician.

DUROGESIC™ patches sold in Europe, Latin America and Asia are not affected by this recall.

FOR IMMEDIATE RELEASE -- Rockville, MD -- February 14, 2008 – Sherwood Brands LLC is voluntarily recalling approximately 400,000 packages of Pokémon® branded "Valentine Cards and Pops™" (Item# 073964209109 and Item# 073964289804), because of reports that metal fragments were found in two lollipops purchased in Florida. There are no reports of injury. People who bite into or swallow a metal fragment could possibly be injured.

The products being recalled are packages of ten and thirty Pokémon branded Valentine cards and lollipops featuring a variety of characters.

Sherwood Brands is advising its distribution network to remove the Pokémon branded Valentine cards and lollipops from the shelves immediately. The product was sold at retailers nationwide.

"Our utmost concern is the safety of our customers. We took immediate action upon learning of this incident and Sherwood is working with the FDA to recall the products," said Amir Frydman, president of Sherwood Brands.

"Pokémon is committed to consumer safety and we’re working closely with our licensee, Sherwood Brands, to investigate this matter completely," said J.C. Smith, Pokémon USA’s director of marketing.

Consumers who have purchased the above products are advised not to consume them and to return them to Sherwood Brands for a full refund. Send affected products to:

Sherwood Brands LLC
Attn: Product Recall
350 Shaw Drive,
Keysville, VA 23947

FOR IMMEDIATE RELEASE -- February 12, 2008 -- See's Candies, Inc. of San Francisco, Calif., is recalling 16-ounce bags of See's Candies Semi Sweet Chocolate Chips because the product may contain undeclared traces of milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

The product was distributed through See's owned retail shops in California, Arizona, Nevada, Oregon, Washington, Utah, Colorado, Idaho, Hawaii, New Mexico, and Illinois. Licensees of See's also sold the product in Nebraska, Iowa, Kansas, Michigan, Texas and internationally in Japan and Hong Kong. See's Mail Order department sold small quantities countrywide.

The product is sold in a black and white See's logo flexible bag. This recall applies to all code dates (30757, 31327, 32067, 33157, and 23397).

There is one reported allergen reaction attributed to this product.

See's Candies confirmed in its investigation that the product was produced on a line that also produces milk chocolates as a follow-up to a consumer contact.

Concerned consumers who have packages of 16-ounce See's Candies Semi Sweet Chocolate Chips should return them to the shops where they were purchased for a full refund. If the product was received through mail order or direct shipment, consumers should contact See's Consumer Affairs at 1 800-789-7337 for product return instructions. Any consumers with questions about this recall should also contact See's Consumer Affairs at 1 800-789-7337.

FOR IMMEDIATE RELEASE -- February 7, 2008 -- Nick and Katie's, Inc. of New Orleans, LA, is recalling the following Nick & Katie's brand products:

Crab Stuffed Mushrooms, net wt 10 oz

Crayfish Stuffed Portabella Mushroom, net wt 10 oz

Stuffed Bell Pepper, net wt 10 oz

Stuffed Crab, net wt 8 oz

Mediterranean Stuffed Artichoke, net wt 16 oz

Stuffed Italian Artichoke, net wt 16 oz

Artichoke Balls, net wt Half Ounce

These products are being recalled because they contain milk, soy, and wheat that was distributed in packaging that did not reveal the presence of milk, soy, and wheat. People who have an allergy or severe sensitivity to milk, soy, or wheat run the risk of a serious or life-threatening allergic reaction if they consume these products.

These products were distributed through retailers from the Greater New Orleans Area including the Northshore to the Greater Baton Rouge Area from January 24, 2008 until February 6, 2008. These products are individually wrapped in clear plastic wrap bearing the following labels: Nick & Katie Ruffino's Crab Stuffed Mushrooms, net wt 10 oz; Nick & Katie Ruffino's Crayfish Stuffed Portabella Mushroom, net wt 10 oz; Nick & Katie Ruffino's Stuffed Bell Pepper, net wt 10 oz; Nick & Katie Ruffino's Stuffed Crab, net wt 8 oz; Nick & Katie Ruffino's Mediterranean Stuffed Artichoke, net wt 16 oz; Nick & Katie Ruffino's Stuffed Italian Artichoke, net wt 16 oz; and Nick & Katie Ruffino's Artichoke Balls, net wt Half Ounce.

There have been no reported illnesses to date.

The omission was found during a routine FDA inspection. Distribution of these products has been suspended while we correct the labels to include all ingredients.

Consumers who have questions or purchased the product may contact Richard Ruffino at (504) 283-8887 for information and return instructi

FOR IMMEDIATE RELEASE -- Napa, CA -- February 11, 2008 -- Annie's Naturals is voluntarily recalling 686 cases of 8 fl oz. bottles of all-natural Shiitake & Sesame Vinaigrette. The product could be mislabeled and may contain soy sauce (contains soy and wheat) and sesame that were not declared on the ingredient statement. People who have an allergy or severe sensitivity to soy run the risk of serious allergic reaction if they consume this product.

There have been no illnesses or injuries reported to date. Anyone concerned about an illness should contact a physician immediately.

Affected product was shipped to grocery and natural food stores in California, Colorado, Connecticut, Florida, Georgia, Indiana, Iowa, Kentucky, Maryland, Michigan, New Hampshire, New Jersey, New York, Oregon, Pennsylvania, South Carolina and Washington, between December 20, 2007 and February 6, 2008.

Consumers can most easily identify impacted product by looking at the product labels – the front label says Shiitake & Sesame Vinaigrette, but the back label and ingredient statement say Low Fat Honey Mustard Vinaigrette. Only dressings with UPC # 0-92325-33319-2 with a Best By Date of 02/20/09/1/E and 02/20/09/2/E are affected.

Organic Shiitake & Sesame Vinaigrette, 16 oz. bottles of Shiitake & Sesame Vinaigrette, and other Annie's Naturals products are not affected by this recall.

The problem occurred during a product changeover when back labels for Honey Mustard Vinaigrette were commingled with back labels for all-natural Shiitake Sesame Vinaigrette. The Honey Mustard Vinaigrette products were unaffected.

Consumers who have purchased 8 fl oz all natural Shiitake & Sesame Vinaigrette are urged to return the product to the place of purchase for a full refund or may call Annie's Naturals Consumer Relations at 1.800.288.1089 to obtain a coupon for a free product.

FOR IMMEDIATE RELEASE -- Grand Rapids, MI -- February 6, 2008 -- Onion Crock of Michigan is recalling its Old Fashion Potato and Minestrone soups to make people aware that while the product is Good and Wholesome, these soups may contain wheat or soy as ingredients not identified on the label.

People who have an allergy or severe sensitivity to soy or wheat run the risk of serious or life threatening allergic reaction if they consume these products

The recalled soups were distributed to restaurants, retail stores, and fund raising companies in mid- and western Michigan.

Old Fashion Potato may be packed in one pound frozen pouches (upc # 643640010772) or in four or eight pound pouches (upc codes # 643640001053) with any Best if used by dates of 7/21/09 or earlier. Minestrone packaged in one pound frozen pouches (upc # 64364001111) or in four or eight pound pouches (upc codes # 643640001138) or with any Best if Used by dates of 7/08/09 or earlier.

No illnesses have been reported to date in connection with this missing labeling.

Concerned consumers who have purchased Old Fashion Potato or Minestrone soups can bring the soups back to where they were purchased for a full refund if they have any concern with wheat or soy allergens. For concerns or questions, please contact Onion Crock of Michigan at 616-458-2922.

• OPA 34171
• OPA 23471
• OAP 17271
• OAP 17671
• OAP 36061
• OAP 36161
• OPA 33961

The recalled product, Olivier Parmesan & Asiago Dip with Garlic & Basil, is packaged in an 11.76 ounce jar. The lot code information is located on the side of the glass jar where there is no label.

Clostridium botulinum is a bacterium which can cause life-threatening illness or death. Symptoms of botulism include: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.

Consumers who find Olivier Parmesan & Asiago Dip with Garlic & Basil, with the affected lot numbers, for sale are encouraged to call the CDPH Complaint Hotline at 1-800-495-3232.

Shiloh Farms Recalls "Shiloh Farms Organic Unhulled Sesame Seeds" Because of Possible Health Risk

FOR IMMEDIATE RELEASE -- New Holland, PA – January 28, 2008 – Shiloh Farms, of New Holland, Pennsylvania, is recalling Shiloh Farms Organic Unhulled Sesame Seeds, 12-oz., because it may be contaminated with Salmonella.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems.Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstance, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. Consumers with the above symptoms should consult their physician.

No illnesses have been reported in connection with this product.

This product comes in a 12 oz blue and white 5” x 8” plastic bag with a Shiloh Farms logo and USDA organic symbol. The UPC bar code number is 047593303545. The firm’s name and address appears on the back of the plastic bag. Product distributed between November 1, 2007 and January 25, 2008 is being recalled. Only product with lot codes 17503 and 17133 are affected.

The contamination was identified when FDA testing revealed the presence of salmonella in a sample of organic sesame seeds from a Shiloh Farms supplier.

The recalled Shiloh Farms product was distributed to a total of 98 health food stores located in New York, Connecticut, New Jersey, Massachusetts, Virginia, Pennsylvania, Maryland and Arkansas.

The company is asking stores to discontinue distribution of this product and to promptly return the product and stock on hand to the company for credit. Consumers should not consume this product and return this product to the point of purchase for a refund.

Consumers with questions may contact Shiloh Farms, (800) 362-6832.

Seoul Shik Poom, Inc. Recalls Frozen Salted Yellow Croaker and/or Frozen Dried Yellow Croaker Because of Possible Health Risk

- January 23, 2008 -- Seoul Shik Poom, Inc. of Hillside, NJ is recalling the following products because they have the potential to be contaminated with Clostridium botulinum, a bacterium, which can cause life-threatening illness or death:

Consumers are warned not to use these products even if they do not look or smell spoiled.

Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision, and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.

Frozen Salted/Dried Yellow Croaker was distributed in New York, New Jersey and Maryland area. It reached consumers through retail stores. This product comes in a clear plastic bag and is individually tied with rope.

The potential for contamination was noted after routine testing. No illnesses have been reported to date in connection with this problem.

Consumers who have purchased these Frozen Salted/Dried Yellow Croaker products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Seoul Shik Poom, Inc. at (908) 810-7230.

Harry and David Issues Nationwide Allergy Alert on Undeclared Peanuts and Other Nuts in Harry and David Giant Cashews

FOR IMMEDIATE RELEASE -- January 22, 2008 -- Harry and David, of Medford, Oregon, is voluntarily recalling approximately 2130 boxes of 4 oz. Harry & David Giant Cashews because they may contain mixed nuts, including peanuts, almonds, pecans and Brazil nuts not declared on the ingredient statement. People who have an allergy or severe sensitivity to these ingredients (peanuts, almonds, pecans and/or Brazil nuts) run the risk of serious or life-threatening allergic reaction if they consume these products.

The affected product was distributed throughout the United States only through Harry and David Stores beginning 11/16/07.

Harry and David is recalling all 4 oz. boxes of Giant Cashews with lot codes 2507 MSL 15:00 through 2507 MSL 18:00 and a use by date of 6/28/08. The lot code and use by date are ink jetted on the bottom of the box. Affected boxes also can be recognized by the price sticker on the bottom, or lower portion of the back, of the box. The price sticker states "Nuts Mixed Nuts Box 4oz". These products are packaged in 4 oz. paperboard boxes with bags of metalized film containing nuts inside. The boxes are olive green with a pale green design in the background.

There have been no illnesses or injuries reported to date. Anyone concerned about an illness/injury should contact a physician immediately.

This problem occurred during a product changeover when packaging for cashews was comingled with packaging for the mixed nuts.

Consumers with product may return it to the any Harry and David retail store for a full refund. Consumers with questions about the recalled product may phone the Harry and David Customer Service division at 800-233-1101, 24 hours a day.

Deli Chef Tri-Bean Salad Recalled From Some Kroger Stores

FOR IMMEDIATE RELEASE -- Cincinnati, Ohio, January 21, 2008 – Inter-American Products, a division of The Kroger Co. (NYSE: KR), today announced a voluntary recall on all codes of Deli Chef Tri-Bean Salad sold from store deli counters in some states because the product has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause a potentially life threatening condition called botulism. Consumers should not consume this product even if it does not look or smell spoiled.

The Tri-Bean Salad was sold at deli counters in stores in Colorado, Illinois, Indiana, Kansas, Kentucky, Michigan, Missouri, Nebraska, Ohio, New Mexico, Utah, Washington, West Virginia, and Wyoming.

The green beans in the Tri-Bean Salad were processed by the New Era Canning Company, which has announced a recall of the beans. The text of the New Era Canning Company Recall can be found on the FDA website at this location: http://www.fda.gov/oc/po/firmrecalls/newera201_08.html.

No illnesses have been reported. No other salad products are affected by this recall.

Customers are encouraged to dispose of the product and should contact the store where the product was purchased to receive a refund.

Consumers with questions or concerns may call Inter-American Products at 1-800-697-2448.

New Era Canning Company Announces New Nationwide Recall of Green Beans and Garbanzo Beans in #10 cans (6 to 7 pound cans)

--- New Era Canning Company of New Era, Michigan is recalling all cans of green beans and garbanzo beans in #10 cans (large cans containing between 6 and 7 pounds) because they may have been processed under conditions which could have led to contamination by Clostridium botulinum bacterium spores, which can cause life-threatening illness or death. The codes on the affected product begin with the numbers “00249,” or the letters “GREEN” or “GARB”. This recall does not include Italian Green Beans because that is a different product.   

Clostridium botulinum bacterium spores have the potential for growth that produces a toxin that causes a potentially fatal form of food poisoning - botulism.  Symptoms of botulism poisoning in humans can begin from 6 hours to 2 weeks after eating food that contains the toxin. Symptoms may include double vision, blurred vision, drooping eyelids, slurred speech, difficulty swallowing, and muscle weakness that moves progressively down the body, affecting the shoulders first, then descending to the upper arms, lower arms, thighs, and calves. Botulism poisoning also can cause paralysis of the breathing muscles, which can result in death unless assistance with breathing (mechanical ventilation) is provided. Individuals who have these symptoms and who may have recently eaten the green beans or garbanzo beans currently under recall or other food products made with these items should seek immediate medical attention.  

The issues were uncovered in a FDA inspection of products that were in the company’s possession.  NO product has tested positive for the toxin and there have been NO cases of botulism reported from these products.

This recall only affects the products in the large #10 cans, the majority of which were potentially sold nationwide to various food service customers.  However these products may also have been purchased by consumers at retail stores. The code on the cans may be embossed (stamped into the metal of the can) or printed in ink on one of the metal can ends.  

Examples of how a code may appear on a can of green beans are: "00249 2BH7FL", "00249 1515 2BH7FL", "GREEN 2BH7FL" or "GREEN 1515 2BH7FL".  (These are not necessarily actual can codes).

Examples of how a code may appear on a can of garbanzo beans are:  "00249 34F7LG", "00249 1515 34F7LG", "GARB 34F7LG" or "GARB 1515 34F7LG".  (These are not necessarily actual can codes).
New Era Canning, in conjunction with the US Food and Drug Administration and the Michigan Department of Agriculture, is thoroughly evaluating all processes and procedures to determine the cause of the problem.

Any food that may be contaminated should be disposed of carefully. Even tiny amounts of toxins ingested, inhaled, or absorbed through the eye or a break in the skin can cause serious illness. Skin contact should be avoided as much as possible, and the hands should be washed immediately after handling the food. Customers who have the product or any foods made with these products should throw them away immediately. Double bag the cans in plastic bags that are tightly closed, then place in a trash receptacle for non-recyclable trash outside of the home. Restaurants and institutions are encouraged to assure that such products are only placed in locked receptacles which are not accessible to the public. Additional instructions for safe disposal can be found at www.cdc.gov/botulism/botulism_faq.htm. Anyone with questions can call FDA at 1-888-SAFEFOOD.

Customers with questions may contact New Era Canning at 1-800-282-9007 Ext. 111.

The following product labels are affected:

Bunny brand, Distributed by Bunn Capitol Company,  Springfield, IL 
Blue Lake mixed and shortcut green beans (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 6444500193).

Classic Sysco brand, Distributed by Sysco Corporation, Houston, TX.
Blue Lake cut green beans, 3 sieve (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 7486510779).
Blue Lake cut green beans, 4 sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 7486510487).
Garbanzo beans (garbanzo beans, water, salt, calcium chloride, EDTA) in 108.0 oz (6 lb. 12 oz.) cans (UPC 7486510484).

Code brand, Distributed by Code, Atlanta, GA.
Mixed & short cut green beans (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 1207310120).
Fancy garbanzo beans without sulfites (garbanzo beans, water, salt, disodium EDTA) in 6 lb. 14 oz. cans (UPC 1207316120).

ComSource brand, Distributed by ComSource, Atlanta, GA. 
Blue Lake cut green beans (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952333).
Blue Lake cut green beans, 3 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952321).
ComSource Medallion Premium Quality brand, distributed by ComSource, Atlanta, GA. 
Fancy Blue Lake cut green beans, 4 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952325).

ComSource Merit Excellence Food Service brand, Distributed by ComSource, Inc, Atlanta, GA.
Cut Blue Lake green beans, 5 sieve (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952327).
Fancy Blue Lake cut green beans, 4 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952325).

ComSource Traditional brand, Distributed by ComSource, Atlanta, GA.
Blue Lake cut green beans, mixed and short cut, (green beans, water, salt) in 101 oz (6 lb. 5 oz.) cans (UPC 5254952359).
Cut Blue Lake green beans, 4 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952427).
Cut Blue Lake green beans, 5 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 5254952429).

Frosty Acres Restaurant's Pride Preferred brand, Packed for F.A.B., Inc., Alpharetta, GA.
Fancy Blue Lake cut green beans, 3 sieve (green beans, water, salt), in 101 oz. (6 lb. 5 oz.) cans (UPC 4820067373).
Cut Blue Lake green beans, 4 sieve (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 4820067445).
Blue Lake cut green beans, 5 sieve (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 4820067451).
Fancy cut Blue Lake green beans (green beans, water, salt), in 101 oz. (6 lb. 5 oz.) cans (UPC 4820067339). 
Fancy cut Blue Lake green beans, 4 sieve (green beans, water, salt), in 101 oz. (6 lb. 5 oz.) cans (UPC 4820067446). 
Mixture of Blue Lake short cut, cut green beans (green beans, water, salt), in 101 oz. (6 lb. 5 oz.) cans (UPC 4820068464).
Fancy garbanzos "chick pea" (garbanzo beans, water, salt, calcium chloride, disodium EDTA) in 111 oz. (6 lb. 15 oz.) cans (UPC 4820068264).

GFS brand, Distributed by Gordon Food Service, Grand Rapids, MI
Fancy Blue Lake cut green beans, 4 sieve (green beans, water, salt) in 6 lb. 5 oz. cans, reorder no. 118737 (UPC 9390111873).
  Cut Blue Lake green beans, mixed sieve, (green beans, water, salt) in 6 lb. 5 oz. cans, reorder no. 273856 (UPC 9390127385).

goodtaste brand, Distributed by New Era Canning in New Era, MI.
Cut green beans (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 3683512340).

Harvest Value brand, distributed by U.S. Food Service, Columbia, MD 
Cut green beans, mixed and short cut, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans, 173619 (UPC 5810803534).
Cut green beans (green beans, water, salt) in 101 (6 lb. 5 oz.) cans, 170524 (UPC 5810801047).
Cut green beans, short cut (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans, 173349 (UPC 5810803538).

Kitchen brand, Distributed by Potato Products, Detroit, MI.
5 sieve- EX.-STD. cut Blue Lake green beans (green beans, water, salt) in 6 lb. 6 oz. cans

Kitchen Essentials brand, Distributed by Gordon Food Service, Grand Rapids, MI.
Cut green beans, mixed sieve, (green beans, water, salt) in 6 lb. 6 oz. cans, reorder no. 156337  (UPC 9390115633).

Monarch brand, Distributed by Reid, Murdoch & Co., Columbia, MD
Extra Fancy Blue Lake cut green beans, 4 sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans, 177039 (UPC 5810811196).
Fancy Blue Lake cut green beans, 3 sieve, (green beans, water, salt) in 101 oz (6 lb 5 oz) cans, 170672 (UPC 5810801040).

Monarch Premium brand, packed for PYA/Monarch, Inc, Greenville, SC.
Fancy Blue Lake cut green beans, 3 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans, 173205  (No UPC code).

Mount Stirling brand, Distributed by Pocahontas Foods USA,  Richmond, VA.
Blue Lake cut green beans, 5 sieve, (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 4156033379).

Necco brand, Packed by New Era Canning Company, New Era, MI.
Cut green beans (green beans, water, salt) in 6 lb. 6 oz. cans (UPC 3683513340).

New Era brand, Distributed by New Era Canning Co, New Era, MI. 
Veri-Green cut green beans (green beans, water, salt, zinc chloride) in 102 oz. (6 lb. 6 oz.) cans (No UPC code).
Cut green beans (green beans, water, salt) in 108 oz. (6 lb. 12 oz.) cans (UPC 3683511340).
Cut Blue Lake green beans, no salt added, (green beans, water) in 102 oz. (6 lb. 6 oz.) cans (No UPC code).
Garbanzo beans (garbanzo beans, water, salt, calcium chloride, EDTA) in 108 oz. (6 lb. 12 oz.) cans (UPC 3683511684).

Nugget brand, Distributed by Nugget, Atlanta, GA.
Green beans, 4 sieve, (green beans, water, salt) in 101 oz. (6lb. 5oz.) (UPC 4410540023).
Cut green beans, 5 sieve (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 4410501930).
Veri-green cut green beans (green beans, water, salt, zinc chloride) in 6 lb. 12 oz. cans (UPC 4410502101).
Mixed short cut green beans (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 4410518838).
Blue Lake cut green beans, 4 sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 4410501989).

Pocahontas brand, Distributed by Pocahontas Foods USA, Richmond, VA. 
Fancy Blue Lake cut green beans, 4 sieve, (Blue Lake green beans, water, salt), 10282, in 6 lb. 5 oz. cans (UPC 4156010282).
Fancy long cut green beans (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 4156010325).
Fancy Blue Lake green beans, 3 sieve, (Blue Lake green beans, water, salt),  10280, in 6 lb. 5 oz.  cans (UPC 4156010280).

Reliance Sysco, Distributed by Sysco Corporation, Houston, TX.
Mixed cut green beans (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 7486512175).
Blue Lake cut green beans, 4 sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans. (UPC 7486512172).
Blue Lake cut green beans, 5 sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans (UPC 7486512174).

Sysco brand, Distributed by Sysco Corporation, Houston, TX.
5096342 Imperial Blue Lake cut green beans, 3 sieve (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 7486512136).
5096359 Imperial Blue Lake cut green beans, 4 sieve (green beans, water, salt) in 6 lb. 5 oz. cans (UPC 7486512137).

US brand Distributed by U.S. FoodService, Columbia, MD.
Cut green beans, mixed sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans, 171132  (UPC 5810801048).
Fancy Blue Lake cut green beans (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans, 173416  (UPC 5810811195).
Fancy Blue Lake cut green beans, 3 sieve, (green beans, water, salt) in 101 oz. (6 lb. 5 oz.) cans, 170672 (UPC 5810801040).
Fancy Blue Lake cut green beans, 4 sieve, (green beans, water, salt) 170232 in 101 oz. (6 lb. 5 oz.) cans, 170672 (UPC 5810801041).
Cut green beans, 5 Sieve, (green beans, water, salt) in 101 oz (6 lb 5 oz) cans, 170675 (UPC 5810801042).

USDA, Food and Nutrition Service, Special Nutrition Programs, Alexandria, VA label.
Cut green beans (green beans, water, salt) in 6 lb. 6 oz. cans (UPC 1500101061).
Garbanzo beans (garbanzo beans, water, salt, calcium chloride, EDTA) in 6 lb. 12 oz. cans (UPC code 1500101089).

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New Era Canning Company (Botulism) Recall Page

Effective January 1, 2008, the following rules apply to the spare lithium batteries you carry with you in case the battery in a device runs low: Spare batteries are the batteries you carry separately from the devices they power. When batteries are installed in a device, they are not considered spare batteries. You may not pack a spare lithium battery in your checked baggage You may bring spare lithium batteries with you in carry-on baggage – see our spare battery tips and how-to sections to find out how to pack spare batteries safely! Even though we recommend carrying your devices with you in carry-on baggage as well, if you must bring one in checked baggage, you may check it with the batteries installed. The following quantity limits apply to both your spare and installed batteries. The limits are expressed in grams of “equivalent lithium content.” 8 grams of equivalent lithium content is approximately 100 watt-hours. 25 grams is approximately 300 watt-hours: Under the new rules, you can bring batteries with up to 8-gram equivalent lithium content. All lithium ion batteries in cell phones are below 8 gram equivalent lithium content. Nearly all laptop computers also are below this quantity threshold. You can also bring up to two spare batteries with an aggregate equivalent lithium content of up to 25 grams, in addition to any batteries that fall below the 8-gram threshold. Examples of two types of lithium ion batteries with equivalent lithium content over 8 grams but below 25 are shown below. For a lithium metal battery, whether installed in a device or carried as a spare, the limit on lithium content is 2 grams of lithium metal per battery. Almost all consumer-type lithium metal batteries are below 2 grams of lithium metal. But if you are unsure, contact the manufacturer! Examples of extended-life rechargeable lithium batteries (more than 8 but not more than 25 grams of equivalent lithium content):
	130 watt-hour “universal” lithium ion battery
	160 watt-hour lithium ion battery for professional audio/visual equipment
GUIDE TO RULES EFFECTIVE JANUARY 1, 2008 Type Of Battery/Batteries In Checked Baggage In Carry-On Baggage: Lithium Metal Battery, Installed in a Device (up to 2 grams lithium) Permitted 1 Recommended 1 Spare Lithium Metal Battery (Not Installed In a Device) (up to 2 grams lithium) (up to 2 grams lithium)   Forbidden Permitted in carry-on baggage 2 Lithium Metal Battery, Spare or Installed   (over 2 grams lithium)   Forbidden Forbidden Lithium-Ion Battery Installed in a Device (up to 8 grams lithium equivalent content) Permitted 1 Recommended 1 Spare Lithium-Ion Battery (Not Installed in a Device) (up to 8 grams lithium equivalent content)   Forbidden Permitted in carry-on baggage 2 “Special Case”   Up to 2 Lithium-Ion Batteries, Spare or Installed (between 8 and 25 grams aggregate lithium equivalent content) Spare Batteries: Forbidden! Installed in Devices: Permitted 1   Spare Batteries: Permitted 2 Installed in Devices: Permitted 1 1. Although you may carry some devices and installed batteries in checked baggage, carrying them in carry-on baggage, when practicable, is preferred. In checked baggage, ensure that devices remain switched off, either by built-in switch/trigger locks, by taping the activation switch in the “off” position, or by other appropriate measures. 2. Be sure to take protective measures to prevent against short-circuits. See our spare battery tips and how-to pages.

Domega International Ltd., Inc Issues Alert on Undeclared Sulfites in "King Chief Brand Dried Kudzu"

FOR IMMEDIATE RELEASE --Brooklyn, N.Y. -- Dec. 12, 2007--- Domega International Ltd., Inc., 98 Bay 35th Street, Brooklyn, NY 11214 is recalling "King Chief Brand Dried Kudzu" because it contains undeclared sulfites.  People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.

The recalled "King Chief Brand Dried Kudzu" is sold in uncoded 6oz. plastic packages and is a product of China.  The product was sold nationwide.

The recall was initiated after routine sampling by the New York State Department of Agriculture and Market Food Inspectors and subsequent analysis by the Department’s Food Laboratory personnel revealed the presence of sulfites in "King Chief Brand Dried Kudzu", 6oz. plastic packages which did not declare sulfites on the label.  The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites. 

No illnesses have been reported to date in connection with this product. Consumers who have purchased "King Chief Brand Dried Kudzu", 6oz. plastic packages should return the product to the place of purchase.  Consumers with questions may contact the company at 1-646-938-7345

Blooming Import Inc. Issues Allergy Alert on Undeclared Sulfites in "Golden Lion Brand Dried Hylocereus Undatus Brltt (Dried Natural Herb)"

FOR IMMEDIATE RELEASE -- Brooklyn, NY -- Dec. 3, 2007 --- Blooming Import Inc., located at 45 Bowne Street, Brooklyn, NY 11231 is recalling “Golden Lion Brand Dried Hylocereus Brltt (Dried Natural Herb)” because it contains undeclared sulfites.  Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.

The recalled “Golden Lion Brand Dried Hylocereus Undatus Brltt (Dried Natural Herb)”, a product of China, is packaged in uncoded in 6 oz heat sealed plastic bags.  There were sold in New York State

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the presence of undeclared sulfites in “Golden Lion Brand Dried Hylocereus Undatus Brltt (Dried Natural Herb)” in packages which did not declare sulfites on the label.  The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics.  Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.

No illnesses have been reported to date to this Department in connection with this problem.  Consumers who have purchased “Golden Lion Brand Dried Hylocereus Undatus Brltt (Dried Natural Herb)” should return it to the place of purchase. Consumers with questions may contact the company at 1-800-680-3838

California Department of Public Health Warns Consumers Not to Drink Metromint Flavored Water

Contact:
Suanne Buggy or Lea Brooks
(916) 440-7259

FOR IMMEDIATE RELEASE -- December 5, 2007 -- Dr. Mark Horton, director of the California Department of Public Health (CDPH), today warned consumers not to drink Metromint brand flavored water because it may be contaminated with a bacterium called Bacillus cereus, a microorganism that may cause vomiting or diarrhea. Soma Beverage Co., LLC., of San Francisco is voluntarily recalling all bottles of Metromint brand flavored water (Peppermint, Spearmint, Orangemint and Lemonmint) with a "Best Before" date prior to 2008/12/21 (Dec. 21, 2008) and produced at its California facility because they may be contaminated with Bacillus cereus. The "Best Before" date is on the shoulder of the bottle.

The product was distributed nationwide to grocery stores, including those in California, and sold on the Internet.

There have been no confirmed illnesses in California associated with this product to date. There is an illness complaint in Illinois that is possibly linked to consumption of this product.

The products were packaged in clear plastic 16.9-ounce bottles with a black M on the front and the lettering "KSA" in a rectangle located on back of the bottle in the lower right-hand corner.

The products were sold at the following locations in Northern California: Albertson's, Andronico's, Berkeley Bowl, BevMo!, Brown and Cole, Central Markets, Cost Plus World Market, Draeger's, Elephant Pharmacy, Fiesta Markets, Fred Meyer, Food Emporium, Haggen, Harmon's (UT), Lunardi's, Marlene's, Super Supplements, Mollie Stone's, New Seasons, PCC, Pharmaca, PW Markets, QFD, Rosauers, Safeway, Thriftway, Top Foods, Town and Country, Uwajimaya, Whole Foods Market, Wild Oaks Market, Yokes and Zupans.

In Southern California, the products are sold at AJ's Fine Foods, Albertson's, Baron's Markets, BevMo!, Bristol Farms, Clark's Nutrition, Cost Plus World Market, Erewhon Market, Fry's, Gelson's, Henry's, Jensen's, Jimbo's Naturally, Lazy Acres, Mother's Market, New Frontiers, One World Fine Foods, Organic To Go, Pacific Coast Greens, Pavillions, Pharmaca, Ralph's, Sprouts, Sunflower, Vitality Juice and Java Bar, Vons, Wally's Win and Spirits, Wild Oats Market and Whole Foods Market. Illness caused by Bacillus cereus may be either a vomiting or a diarrheal type. The vomiting type is characterized by nausea and vomiting within 30 minutes to six hours after consumption of contaminated foods. Duration of symptoms is generally less than 24 hours. The diarrheal type usually includes onset of abdominal cramps and watery diarrhea six to 15 hours after consumption of contaminated food. Symptoms may last for 24 to 48 hours.

Consumers in possession of the recalled product should discard it or return it to the point of purchase. Individuals who have become ill from drinking the product should contact their health care provider for evaluation.

Consumers with questions may contact the company at (415) 979-0781, Ext. 101

Cedarlane Natural Foods Issues Allergy Alert on Undeclared Casein in Cedarlane Low Fat Bean Rice and Cheese style Burritos

FOR IMMEDIATE RELEASE -- December 12, 2007 -- Cedarlane Natural Foods of Carson, California is conducting a voluntary recall of Cedarlane Low Fat Bean Rice & Cheese style Burritos because they contain undeclared casein, a milk protein. People who have an allergy, or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. No illnesses have been reported to date.

The reason for this voluntary recall is due to the fact that an allergen, casein, (a milk protein) was not noted on the printed packaging of the individual units. Specifically, the printed outer carton contains the word casein in the allergen statement. The individually wrapped burrito however does not reference casein in the allergen statement. The labeling error was detected by a routine review at Cedarlane Natural Foods as well as the Food and Drug Administration.

Cedarlane Low Fat Bean Rice & Cheese Style Burritos are available in a 6 oz plastic film wrapped packaging as well as cartons of an 8 count, 6 oz family pack. The affected open code dates are from "062808A" (June 28, 2008) through "082908A" (August 29, 2008) and is located on the bottom right, after the heating instructions, of the print plastic wrap of the individual burrito. The open code date of the outside printed carton is similar to that of the individual units but without the 'A' and can be found on the right hand side panel, near the bottom of the carton.

Cedarlane Low Fat Bean Rice & Cheese style Burritos are distributed through all 50 states (U.S). Consumers that possess this product with the respective open code dates are advised by Cedarlane Natural Foods to return the product to the store of purchase for a full refund. Refunds can be obtained until June 1, 2008.

Grocers and distributors have been advised by Cedarlane Natural Foods to withdraw the product with respective open code dates listed above from sale and hold it for pick up from the company. Consumers with any questions may contact the company either by telephone at (800) 826-3322 and speak with Linda Manzo, extension 800, or by e-mail at we-care@cedarlanefoods.com

Harry & David recalls Harry & David Bake Shop Cookie Mixes in Three Flavors: Oatmeal Chocolate Chip, Chocolate Peanut Butter and Cranberry Vanilla Chip for Undeclared Nut, Milk and/or Sulfite Allergens

FOR IMMEDIATE RELEASE -- December 7, 2007 -- Harry & David of Medford, Oregon, is voluntarily recalling approximately 50 jars each of the Oatmeal Chocolate Chip, Chocolate Peanut Butter and Cranberry Vanilla Chip cookie mixes because they may contain coconut, peanuts, milk and/or sulfites not declared on the ingredient statement. This product was made for Harry & David by Sisters’ Gourmet, Inc., a co-packer. People who have an allergy or severe sensitivity to these ingredients (coconuts, peanuts, milk and/or sulfites) run the risk of serious or life-threatening allergic reaction if they consume these products.

The products are packaged in 1 lb. 2 oz or 1 lb. 5 oz clear jars. The nutrition and ingredient information is contained inside hang tags attached to the top of the jars.

The recalled items may be quickly identified by checking for a match of the flavor description on the hang tag at the top of the jar with the flavor description on the price sticker on the bottom of the jar. Jars being recalled have flavor descriptions that DO NOT match.

Harry & David is recalling all Oatmeal Chocolate Chip cookie mix jars with bottom price stickers stating "Cookie Mix PB" or "Cookie Mix WC Cran". The potentially affected lot codes are 111207 or 110907 respectively.

Harry & David is recalling all Chocolate Peanut Butter cookie mix jars with bottom price stickers stating "Cookie Mix Oatmeal CC" or "Cookie Mix WC Cran". The potentially affected lot codes are 111407 or 110907 respectively.

Harry & David is recalling all Cranberry Vanilla Chip cookie mix jars with bottom price stickers stating "Cookie Mix Oatmeal CC" or "Cookie Mix PB". The potentially affected lot codes are 111407 or 111207 respectively.

The lot codes are on stickers on the bottom of the jars.

The cookie mixes were distributed exclusively throughout the United States in Harry & David Stores, beginning on November 27, 2007.

There have been no injuries reported to date. Anyone concerned about a potential illness associated with this product should contact a physician immediately. This problem occurred when hang tags were applied to the wrong flavor of cookie mix.

Consumers with questions about the recalled product may phone the Customer Service division at 800-233-1101, 24 hours a day. Customers may arrange for refunds through this number as well.

Harry & David recalls Harry and David Moose Munch Confection tubs in two flavor combinations: Milk & Dark Chocolate, White Chocolate Macadamia and Peanut Butter, Milk Chocolate, Macadamia Nut for undeclared nut allergen (Nov. 21)
Fri, 23 Nov 2007 11:21:00 -0600

Harry & David Operations Corp., of Medford, Oregon, is voluntarily recalling approximately 5880 tubs of the Milk & Dark Chocolate, White Chocolate Macadamia because they may contain macadamia nuts not declared on the ingredient statement, and 4400 tubs of the Peanut Butter, Milk Chocolate, Macadamia Nut because they may contain macadamia nuts and peanuts not declared on the ingredient statement. People who have an allergy or severe sensitivity to these nuts (macadamia or peanut) run the risk of serious or life-threatening allergic reaction if they consume these products.

Charlemagne Chocolatiers Issues Allergy Alert on Undeclared Milk Protein in Charlemagne Dark Chocolate Organic Bars

Contact:
Belgium ’s Best Chocolates, Inc
781-283-5787

FOR IMMEDIATE RELEASE -- November 20, 2007--- Charlemagne Chocolatiers of Belgium is voluntarily recalling its dark chocolate organic bars currently on the US market, because it may contain undeclared milk protein. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. Charlemagne Organic Bars are distributed in the US by Belgium’s Best Chocolates, Inc. and were shipped to retail stores in the following states: MI, CA, NJ, NY and MA. Approximately 5000 units of dark Charlemagne organic chocolate bars were distributed. The following chocolate bars are affected:

- Charlemagne Dark with Coffee 50 gr.(1.75 oz.) (UPC= 5 425001 204038)
- Charlemagne Dark with Cinnamon 50 gr.(1.75 oz.) (UPC= 5 425001 204052)
- Charlemagne Dark with Orange 50 gr.(1.75 oz.) (UPC= 5 425001 204021)
- Charlemagne Dark with Green tea 50 gr.(1.75 oz.) (UPC= 5 425001 204045)
- Charlemagne Plain Dark with Belize Chocolate. 50 gr.(1.75 oz.) (UPC= 5 425001 204014)

No illnesses have been reported to date in the US. The Charlemagne Organic dark chocolate bars were tested for milk protein in the US by FDA after a recall was initiated in Canada. The organic dark chocolate bars were distributed in packaging that did not list milk protein in the ingredients or allergen statement.

Consumers that have purchased Charlemagne Organic Dark chocolate products can return it to the place of purchase for a full refund. Consumers with questions may contact the US distributor at 1-877-INDULGE.