Healthy People Co. Issues a Voluntary Recall of Specific Lots of the Dietary Supplements Found to Contain Undeclared Drug Ingredients

Healthy People Co. announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplements sold under the brand names Healthy People Co. specific to the following Lot Numbers.

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California Firm Recalls Prepared Sandwiches that Contain Hard-Cooked Eggs

GH Foods CA, LLC was notified by their supplier that the eggs supplied to them were from Michael Foods, Inc, who recalled Hard-Cooked eggs due to potential contamination by Listeria monocytogenes.

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Greencore, USA – Cincinnati, Recalls Egg Salad Sandwiches with Brand Name Quick Café and Take Away Café because of Possible Health Risk

Greencore, USA is recalling approximately 550 pounds of egg salad sandwiches. The sandwiches contain eggs manufactured by Michael Foods Inc that are the subject of a previous recall due to possible contamination with Listeria Monocytogenes.

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Cephalon, Inc. issues a voluntary nationwide recall of Treanda® (bendamustine HCL) for Injection 25mg/Vial Due to Particulate Matter

Cephalon, Inc. is voluntarily recalling Treanda® (bendamustine HCL) for Injection 25mg/8mL; lot TB30111, expiration date 12/2012. This product lot is being recalled due to the presence of particulate matter found in a single vial, which has been identified as glass fragments

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Perfect Image Solutions, LLC Issues Voluntary Recall of Unapproved Product Due to Potential Health Risk

Perfect Image Solutions, LLC is voluntarily recalling all lots of Men’s Minoxidil 15% Azelaic 5% Hair regrowth topical, 60mL; Men’s Minoxidil 10% Azelaic 5% Hair regrowth topical, 60mL; Men’s Minoxidil 5% Azelaic 5% Hair regrowth topical, 60mL; Women’s Minoxidil 3% Azelaic 5% Hair regrowth topical, 60mL; and Hair regrowth shampoo enhanced with Ketoconazole and salicylic acid, 180mL, to the consumer level. The products are deemed “unapproved new drugsâ€? under the law and U.S. Food and Drug Administration regulations and may present potential health hazards.

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Carefusion Provides Update on Voluntary Recall of Neurilogical Monitoring Software and Devices

CareFusion issued the following update regarding its voluntary recall of the Nicolet® Cortical Stimulator Control Unit, Nicolet® C64 Stimulus Switching Unit (SSU) Amplifier and NicoletOne Software with Cortical Stimulator License. The FDA has classified this action as a Class I recall.

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JKS Wholesale SVCS, Allergy Alert On Undeclared Milk Allergens In "Torta de Pan" Date Code 02/15/2012

JKS Wholesale SVCS INC, of Beltsville, MD is recalling its 16 oz. packages of “Torta de Pan� because they may contain undeclared milk allergens

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Rich Products Corporation expanded its voluntary recall on January 12, 2012, of Vanilla Pre-Soaked Sponge Cake to include the 8�…

Last week, Rich Products Corporation expanded its January 5, 2012 recall of one fourth Sheet Vanilla Soaked Sponge Cake Artificially Flavored to include the 8 inch Vanilla Flavored Pre-Soaked Sponge Cake Artificially Flavored (Product Code: 62938) because of the possibility that small plastic fragments from the packaging were contaminating the product.

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USA Far Ocean Group Inc. Issues Voluntary Nationwide Recall of Vagifresh Ball and Vagifresh Gel, Marketed Individually or Under a Mixed Package Named…

USA Far Ocean Group Inc. (U.S.A

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Winn-Dixie Issues Voluntary Recall On LEASA Brand Sprouts Due To Potential Salmonella Exposure

Winn-Dixie Stores, Inc., today announced an immediate Class I voluntary recall of all LEASA Living Alfalfa Sprouts sold in the 6 oz. package with a UPC code of 7546555912

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