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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:

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:

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:

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:

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:

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.

Tropifresh, Inc. Recalls Whole Cantaloupe Products Because of Possible Health Risk

 

FOR IMMEDIATE RELEASE -- Los Angeles, CA -- March 26, 2008 --- Tropifresh, Inc. of Los Angeles, CA is recalling Agrolibano’s Produce Brand whole Cantaloupes because they appear 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.

Whole cantaloupe fruits subject to this recall carry a “Mike’s Melons” sticker or may be unlabeled because this sticker has fallen off. Whole cantaloupes fruits subject to this recall were sold in approximately 1100 pound cardboard bin containers and were distributed to wholesalers in Southern California, Pennsylvania and Canada.

No illnesses have been reported to Tropifresh, Inc. to date.

These cantaloupe products were supplied from Agropecuaria Montelibano, a Honduran grower and packer, to Tropifresh. This recall was initiated when the U.S. Food and Drug Administration  issued an import alert regarding cantaloupe from this grower, because, based on current information, fruit from this company appears to be associated with a Salmonella Litchfield outbreak in the United States and Canada.

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.

 

 

Spokane Produce Recalls Cut Cantaloupe Products Because of Possible Product Risk

FOR IMMEDIATE RELEASE --Spokane, WA -- March 28, 2008 --- Spokane Produce, Inc. of Spokane, Washington is recalling Garden Patch, Yokes, and Rosauers Classic labels of various products of fresh cut and cut fruits containing cantaloupe, 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), endocaritis and arthritis.

Products recalled by Spokane Produce include the following items containing cut cantaloupe:

Cantaloupe Chunks and Pieces
Sizes: 5oz, 8oz., 11oz, 12oz.,16oz., 21oz, 24oz., 32oz., 48oz., 64oz. & 5 lb.

Melon Medley
Sizes: 6oz., 8oz., 11oz., 12 oz., 16oz., 23.oz., 24oz., 32oz., 48oz., 64oz.

Mixed Melon Cantaloupe-Honeydew
Sizes: 4oz., 5oz., 8oz., 11oz., 16oz., 22oz., 24oz., 32oz., 48oz.

Fruit Medley
Sizes: 5oz., 8oz., 11oz., 12oz., 16oz., 23oz., 24oz., 32oz., 48oz., 64oz.

Fruit Medley with Strawberries
Sizes: 16oz., 24oz.

Mixed Melon and Fruit
Sizes: 6oz., 11oz., 16oz., 24oz.

Fruit Trays
Sizes: 40oz., 48oz., 75oz.

Products are packed in plastic cups or clamshells and distributed under the Garden Patch, Yokes, or Rosauers Classic labels. Products are coded with a “Best used by” dates up to and including 03/26/08.

The above products were distributed through retail stores in Washington, Idaho, Montana, Oregon, and Wyoming. Products are packed in plastic cups or clamshells and distributed under the Garden Patch, Yokes or Rosauers Classic labels.

No illnesses reported to date have been directly linked to the above-mentioned products.

The cantaloupe products were supplied from Agropecuaria Montelibano, a Honduran grower and packer, to Spokane Produce. This recall was initiated when the U.S. Food and Drug Administration issued an import alert regarding cantaloupe from this grower, because, based on current information, fruit from this company appears to be associated with a Salmonella Litchfield outbreak in the United States and Canada.

Consumers who have purchased these products are urged to return them to the place of purchase. Customers with questions may contact Dan Petek of Spokane Produce at 509.710.8301.

　

Chiquita Brands International, Inc. Recalls Whole Cantaloupes Grown by Agropecuaria Montelibano, Honduras, Due to Possible Health Risk

Contact:

FOR IMMEDIATE RELEASE -- Cincinnati, OH -- March 27, 2008 -- Chiquita Brands International, Inc. today announced a voluntary recall of cantaloupes grown, packed and shipped by an independent third-party grower, Agropecuaria Montelibano in Honduras. The product was distributed to customers nationwide and is being recalled because they have the potential to 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. Symptoms of food-borne Salmonella infection include nausea, vomiting, fever, diarrhea, and abdominal cramps. Individuals who have recently eaten cantaloupe and experienced any of these symptoms should contact their health care professional.

The cantaloupes were distributed for sale throughout the US and Canada in cardboard cartons with the brands "Mike's Melons," "Mayan Pride" and "Chiquita" all showing "PRODUCE OF HONDURAS" printed on each of the side panels of the carton. The address of the shipper appears on one end panel of the carton as follows:

GROWN, PACKED AND SHIPPED BY:
AGROPECUARIA MONTELIBANO
SAN LORENZO, VALLE, HONDURAS

Chiquita advises that U.S. grocers, food service operators and produce processors remove from their stock all recall product. Chiquita also advises consumers who have recently bought cantaloupes to check with the place of purchase to determine if the fruit came from this specific grower and packer. If so, consumers should throw away the cantaloupes.

Consumers with questions may contact the company at (800) 242-5472.

　

Bounty Fresh, LLC. Recalls Cantaloupe Because of Possible Health Risk

Contact:

FOR IMMEDIATE RELEASE -- Miami, FL -- March 27, 2008 -- Bounty Fresh, LLC, has recalled cantaloupes from Agropecuaria Montelibano, a Honduran grower and packer because the U.S Food and Drug Administration ("FDA") has determined, based on current information, that cantaloupe fruit from this company 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.

The recalled product was distributed nationwide to wholesalers and grocery stores. Whole cantaloupe fruits subject to this recall are packed three melons in a sleeve under the brand "Chestnut Hill Farms" and one melon per sleeve under the "Perfect Melon" brand. Individual melons are not labeled, but sleeves contain tags that say either "Perfect Melon" (one count) or "Chestnut Hill Farms" (3 count). Whole cantaloupe fruits subject to this recall were sold in boxes marked with the following text: "Cantaloupe, "Chestnut Hill Farms" (3 count) or "Perfect Melon" (one count) , Produce of Honduras, Grown, Packed and Shipped by Agropecuaria Montelibano, San Lorenzo, Valle, Honduras". All boxes also contain the Chestnut Hill Farms logo.

This recall has been initiated based on the FDA"s determination, based on current information, that cantaloupe fruit from the referenced grower/packer appears to be associated with a Salmonella Litchfield outbreak in the United States and Canada.

Consumers who have recently bought whole cantaloupes from this specific grower and packer should destroy these products immediately. Consumers with questions may contact Raul Romero, Bounty Fresh, LLC at 305-592-6969.

　

Simply Fresh Fruit Announces Nationwide Recall of Some Fresh Cut Fruit Products Containing Cantaloupe Due to Possible Salmonella Contamination

FOR IMMEDIATE RELEASE -- Los Angeles, California -- March 27, 2008 --- Simply Fresh Fruit, of Los Angeles, California is recalling selected fresh cut fruit products which may contain cantaloupe which has the potential to be contaminated with Salmonella. On March 26, 2008, Simply Fresh was requested by its supplier, Tropifresh, Inc to recall products produced with cantaloupe from Agropecuaria Montelibano. Simply Fresh had begun to recover this product earlier, on March 24, based on a notice published
By the U.S. FDA.

The products being recalled include: Simply Fresh Fruit Brand food service Fruit Mix in Syrup products dated “sell by 4 – 18 08” or earlier, food service Cantaloupe Chunks in Syrup products dated “sell by 4 – 08 8” or earlier, and retail and club store Simply Fresh, Fresh Cut Fruit Brand containing cantaloupe dated “sell by 3 – 29 8”or earlier. Retail and club store products involved were removed from sale prior to Monday, March 24. Foodservice distributors who sell their own brand, have been notified, and are recalling the products involved. Foodservice products are packed in plastic pails or jars, and retail products are packed in plastic trays.

Symptoms of food borne Salmonella infection include nausea, vomiting, fever, diarrhea, and abdominal cramps. In persons with poor health or weakened immune systems, Salmonella can invade the bloodstream and cause life-threatening infections.

We are unaware to date of any illnesses that may be associated with any products containing cantaloupe, sold by Simply Fresh Fruit, or its distributors.

Food Service establishments who have any of the products involved should contact their supplier for disposition instructions. Consumers with questions may contact Simply Fresh Fruit at (323) 586-0000.

　

T.M. Kovacevich International, Inc. Recalls Cantaloupe Because of Possible Health Risk

FOR IMMEDIATE RELEASE -- Philadelphia, PA -- March 25, 2008 --- T.M. Kovacevich International, Inc. of Philadelphia, PA is recalling cantaloupes which it purchased from Agropecuaria Montelibano, a Honduran grower and packer, because the U.S. Food and Drug Administration (“FDA”) has determined, based on current information, that cantaloupe fruit from this company 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.

The recalled product was distributed to wholesalers and processors in Georgia, Florida, Massachusetts and New Jersey, and may have reached consumers through grocery stores, restaurants, or other similar channels. Whole cantaloupe fruits subject to this recall carry a “Mike’s Melons” sticker or may be unlabeled because this sticker has fallen off. Whole cantaloupe fruits subject to this recall were sold in boxes marked with the following text: “Cantaloupe, Mike’s Melons, Produce of Honduras, Grown, Packed and Shipped by Agropecuaria Montelibano, San Lorenzo, Valle, Honduras”.

We are unaware to date of any illnesses that may be associated with any cantaloupes sold by our company.

This recall has been initiated based on the FDA’s determination, based on current information, that cantaloupe fruit from the referenced grower/packer appears to be associated with a Salmonella Litchfield outbreak in the United States and Canada.

Consumers who have recently bought whole cantaloupes from this specific grower and packer should destroy these products immediately. Consumers with questions may contact George Manos of T.M. Kovacevich International, Inc. at (215) 336-3160.

 

 

FOR IMMEDIATE RELEASE -- Los Angeles, CA -- March 26, 2008 --- Tropifresh, Inc. of Los Angeles, CA is recalling Agrolibano’s Produce Brand whole Cantaloupes because they appear 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.

Whole cantaloupe fruits subject to this recall carry a “Mike’s Melons” sticker or may be unlabeled because this sticker has fallen off. Whole cantaloupes fruits subject to this recall were sold in approximately 1100 pound cardboard bin containers and were distributed to wholesalers in Southern California, Pennsylvania and Canada.

No illnesses have been reported to Tropifresh, Inc. to date.

These cantaloupe products were supplied from Agropecuaria Montelibano, a Honduran grower and packer, to Tropifresh. This recall was initiated when the U.S. Food and Drug Administration  issued an import alert regarding cantaloupe from this grower, because, based on current information, fruit from this company appears to be associated with a Salmonella Litchfield outbreak in the United States and Canada.

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.

 

　

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."

 

 

New BCN Trading Inc. Issues Allergy Alert on Undeclared Sulfites in Asian Boy Sweet Ginger

- New BCN Trading Inc. of South Plainfield, NJ is recalling 7 oz. plastic tubs of Asian Boy Brand Dried Ginger because the product 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. No illnesses have been reported to date in connection with this product.

The Asian Boy Brand Dried Ginger, a product of Vietnam, was distributed to retail stores in NJ, NY, FL, MD, VA, CT, MA, OH and PA in an uncoded 7 oz. plastic tub.

The recall was initiated after sampling by New York State Dept. of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 7 oz. plastic tubs of Dried Ginger which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions is some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulties. Analysis of the Asian Boy Brand Dried Ginger revealed that it contained 27.3 mg of sulfites per serving.

No illnesses or allergic reactions involving this product have been reported to date. Consumers who have purchased 7 oz. plastic tubs of Asian Boy Brand Dried Ginger are urged to return the product to the place of purchase for a full refund. Consumers with questions may contact the company at 908-757-2500

 

Summit Import Corporation Issues an Alert on Uneviscerated Fish

 

FOR IMMEDIATE RELEASE -- February 12, 2008 -- Summit Import Corp. 100 Summit Place, Jersey City, NJ 07305 is recalling all packages of Sum Cheong Lung brand Dried Fish discovered by New York State Dept. of Agriculture and Markets Food Inspectors during a routine inspection and subsequent analysis of the product by Food Laboratory personnel confirming that the fish had not been eviscerated prior to processing.

This product may be contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food-borne illness.

The sale of this type of fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning. Symptoms of botulism include blurred or double vision, general weakness, poor reflexes, difficulty swallowing and respiratory paralysis.

The recalled Sum Cheong Lung brand Dried Fish comes in an uncoded 12 oz. plastic bag and is a product of China. Dried Fish was sold in New York State.

No illnesses have been reported to date in connection with this problem. Consumers who have Sun Cheong Lung brand Dried Fish are advised not to eat it, but should return it to the place of purchase. Consumers with questions may contact the company at 201-839-2882.

　

Pierre’s Ice Cream Company Issues Allergy Alert on its Homestyle Brand of Dutch Chocolate Ice Cream for Undeclared Peanut Butter Cup Candies

-- 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

　

　

　

Nutri-Foods Recalls "Organic Sesame Seeds Natural - Unhulled" Because of Possible Health Risk

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.

　

Rocky Mountain Popcorn Company Issues Recall of Low Fat Caramel Popcorn (in the green bag) 9 oz.

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

　

Dreyer's Issues Voluntary Recall of Slow Churned® Light Caramel Delight and Butter Pecan Ice Cream Flavors for Undeclared Pecans