Quinault Tribal Enterprise Recalls All Canned Seafood Products Because of Possible Health Risk

May 3, 2011

Quinault Tribal Enterprise of Taholah, WA recalls all canned seafood products due to potentially harmful and even fatal health risks.  The canned seafood products are being recalled as a result of inadequate processing according to the U.S. Food and Drug Administration’s low-acid canned food regulations. Canned seafood that is not processed following those food safety requirements may be contaminated with harmful microorganisms that can cause serious and possibly life-threatening illness. 

Simply Asia Foods Recalls Three Flavors of Thai Kitchen Rice Noodle Carts and One Flavor of Simply Asia Noodle Bowl Due to Undeclared Milk Ingredient

May 3, 2011

 Simply Asia Foods, LLC recalls Thai Kitchen® Noodle Carts (Sweet Citrus Ginger, Thai Peanut, and Spicy Thai Basil) and Simply Asia® Noodle Bowl (Roasted Peanut) due to an undeclared milk ingredient.

Bristol-Myers Squibb Recalls Coumadin (Warfarin Sodium) Crystalline 5 mg Tablets, Lot Number 9H49374A

May 3, 2011

Bristol-Myers Squibb is recalling one lot of 1,000-count bottles of Coumadin® (warfarin sodium) Crystalline 5 mg tablets. Bottles of 1,000 tablets are distributed to pharmacies for further dispensing to patients in prescription quantities. The lot number affected in the U.S. is 9H49374A with an expiry date of September 30, 2012. The recall is a precautionary measure based on the company’s testing of tablets from a returned bottle. A single tablet was found to be higher in potency than expected.

Coumadin is prescribed to treat or prevent blood clots. A decrease of active ingredient may increase the risk of clots which could lead to heart attack or stroke and if there is too much active ingredient, there is an increased risk of bleeding.

Defibtech Recalls DDU-100 series AEDs: Automatic External Defibrillators (AED)

May 3, 2011

Recalled Defibtech AEDDefibtech, LLC has recalled about 65,885 DDU-100 series semi-automatic external defibrillators (AEDs) sold in the United States under the brand names Lifeline AED and ReviveR AED. These recalled defibrillators may, in rare cases, cancel shock while charging, which could cause a failure to resuscitate the patient.

Grape Tomatoes Recalled Because of Salmonella Risk

May 3, 2011

Six L’s of Immokalee, FL has recalled one lot of grape tomatoes because they may be contaminated with Salmonella. The exact strain of Salmonella has not been determined and no illnesses have been reported as of the date of this recall.

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