The U.S. Department of Justice, on behalf of the U.S.
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FDA Takes Action Against Maryland Veal Calf Dealer
On November 19, 2009, In Food and Drug Administration, By admin
On November 19, 2009, In Food and Drug Administration, By admin
Nassau Candy Distributors of Hicksville, New York, is voluntarily recalling possibly unlabeled pegable snack tubs because they contain the following undeclared allergens; Tree Nuts {Almonds}, Soy and Milk and may contain the following undeclared allergens Peanuts, other Tree Nuts {brazil nuts, walnuts, filberts, hazelnuts, pecans, pistachios, macadamia nuts, cashews and coconut}. People who have an allergy to any of these specific types of allergens run the risk of serious or life-threatening allergic reaction if they consume these products…
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Nassau Candy Issues Nationwide Allergy Alert Because Of Possible Undeclared Allergens on their Tasty Dish Snack Tubs of Chocolate Almonds, Chocolate Raisins and Sour Neon Worms
On November 19, 2009, In Food and Drug Administration, By admin
The U.S. Food and Drug Administration today completed a coordinated, weeklong, international effort, called the International Internet Week of Action (IIWA), intended to curb illegal actions involving medical products.
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FDA Issues 22 Warning Letters to Web site Operators
On November 18, 2009, In Food and Drug Administration, By admin
Patients should avoid using the stomach acid reducer Prilosec/Prilosec OTC (omeprazole) with the anti-clotting drug Plavix (clopidogrel), the U.S. Food and Drug Administration warned on Nov. 17.
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FDA Announces New Warning on Plavix: Avoid Use with Prilosec/Prilosec OTC
On November 13, 2009, In Food and Drug Administration, By admin
The Food and Drug Administration’s Center for Food Safety and Applied Nutrition (CFSAN) today released a report from the Institute of Food Technologists (IFT), which recommends clear objectives be set for all users of a simpler, globally accepted food supply chain that can benefit from existing commercial systems.
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New Report Recommends Enhanced Food Tracing Guidelines
On November 13, 2009, In Food and Drug Administration, By admin
IDS Sports announced today that it is conducting a voluntary nationwide recall of five of the company’s dietary supplement products sold under the following names: Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR. The Food And Drug Administration (FDA) has notified IDS Sports that the recalled products contain the following undeclared substances, which FDA considers to be steroids: “Madol,” “Turinabol,” “Superdrol,” and/or “Androstenedione.”
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IDS Sports Conducts a Voluntary Nationwide Recall of Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR
On November 13, 2009, In Food and Drug Administration, By admin
Herbal Products, Inc. has been informed by the Food and Drug Administration (FDA) that Pai You Guo, a weight loss dietary supplement, sold and marketed by the firm contains undeclared drug ingredients.
On November 13, 2009, In Food and Drug Administration, By admin
The U.S. Department of Justice, on behalf of the U.S
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FDA Takes Action against Seafood Processing Company, Executives
On November 12, 2009, In Food and Drug Administration, By admin
The U.S. Food and Drug Administration has approved the use of the CSL Limited’s 2009 H1N1 influenza vaccine to include children ages 6 months and older.
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FDA Expands Approved Use of H1N1 Vaccines to Include Infants and Children
On November 5, 2009, In Food and Drug Administration, By admin
PetSmart (NASDAQ: PETM) is voluntarily recalling two Dentley’s Beef Hoof products for potential salmonella contamination.