Sirob Imports, Inc. of Lindenhurst, NY, is recalling 16 oz vacuum packed bags of Strawberry Farm Sun Dried Tomatoes because they contain undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
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Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen
The Kroger Co. said today it is recalling select containers of Kroger Deluxe Chocolate Paradise Ice Cream sold in 17 states because it may contain tree nuts not listed on the label. Customers should return the product to stores for a full refund or replacement.
Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk
Bimbo Bakeries USA, Inc. is recalling Bimbo brand Soft White Bread (1 lb. 4 oz. or 567 grams) sold in California, Idaho, Oregon and Washington because it may contain undeclared milk. People who have an allergy to milk run the risk of life threatening or serious allergic reaction if they consume the product.
Domega NY International Co., LTD Issues Allergy Alert on Undeclared Egg in Fuma Custard Pie
DOMEGA NY INTERNATIONAL CO. LTD 4820 2nd AVE BROOKLYN NY 11232 is recalling FUMA CUSTARD PIE because it may contain undeclared eggs. Consumers who are allergic to eggs may run the risk of serious or life-threatening allergic reactions if they consume this product.
P&G Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1)
The Procter & Gamble Company (P&G) (NYSE:PG) is voluntarily recalling specific lots of its Iams canned cat food in North America as a precautionary measure. Diagnostic testing indicated that the product may contain insufficient levels of thiamine (Vitamin B1), which is essential for cats. Cats that were fed these canned products as their only food are at greater risk for developing signs of thiamine deficiency.
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Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED® and ReviveR AEDTM
Defibtech, LLC, is
initiating a voluntary recall of 5,418 DBP-2800 Battery Packs used in the Lifeline AED®
and ReviveR AEDTM (semi-automatic external defibrillators). This recall affects all DBP-
2800 Battery Packs shipped prior to June 4, 2007. In rare instances, when the AED is
used with an affected battery pack, the AED may falsely detect an error condition during
charging for a shock, then cancel charge and not provide therapy. Defibtech determined
the need for this recall after learning of four reports from end users of this malfunction
during patient use.
West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk
West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured Ondansetron in 5% Dextrose Injection, supplied in 32mg/50mL Single-Use Plastic Bag Containers and Metronidazole Injection 500mg/100ml USP in Flexible IV Plastic Bag Containers. Claris recently received reports of the presence of floating matter and non-sterility in Ondansetron and Metronidazole. Non-sterile products administered intravenously may cause infections which could be fatal especially in patients who are immuno-compromised.
Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
Pfizer Inc is voluntarily recalling Metronidazole, Ciprofloxacin and Ondansetron IV Products due to the presence of floating matter and non-sterility discovered by the manufacturer Claris Laboratories. Non-sterility of a product administered via the intravenous route has the potential to result in infections, which could be fatal, especially in patients who are immunocompromised. Metronidazole and Ciprofloxacin injections are intravenous antibiotics used to treat infections.
Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences
Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of all lots of ondansetron injection in 5% dextrose 32mg / 50 mL (NDC number 25021-776-50) manufactured by Claris Lifesciences and distributed by Sagent. The lot numbers being recalled are: A090309, A090310, A090311 and A090312, which were distributed to hospitals, wholesalers and distributors nationwide from August 2009 through May 2010. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery and is supplied in a single dose plastic container.
Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico
Eastern Fish is alerting consumers that Hannaford Supermarkets and Bloom brands of frozen raw extra jumbo (16/20) shrimp in 16 oz packages, as well as these brands of shrimp from the full-service seafood cases, labeled as product of Mexico, sold May 4 through June 4 at Hannaford Supermarkets and sold April 8 through June 4 at Bloom grocery stores, are subject to a voluntary recall because the products may contain undeclared sulfites. People who have an allergy or sensitivity to sulfites risk an allergic reaction if they consume these products.