Avon Heights Mushrooms, in full cooperation with the FDA is recalling certain packages of fresh packaged spinach. The brands include Krisp Pak 1 Ooz bags, Better Brand 10oz.bags, and Avon Heights 4-2.51b bags.
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Category Archives: Food & Drug Recalls
IKARIA® Issues Notice of Completed Remediation For INOMAX® DS Drug-Delivery System
Ikaria, Inc. announced today that it has completed a remediation action for its INOMAX® DS drug-delivery systems related to a fretting corrosion. This class I recall notice is being issued at the direction of the U.S. Food and Drug Administration (FDA). No further action is necessary.
Sirocco Enterprises, Inc. Issues Allergy Alert On Undeclared Soy And Wheat In Pat O’Brien’s Bloody Mary Cocktail Mix
Sirocco Enterprises, Inc, Jefferson, LA is recalling its 33.8 fluid ounce (1 Liter) bottles of Pat O’Brien’s Bloody Mary Cocktail Mix because it contains undeclared soy and wheat. People who have allergies to soy and wheat run the risk of serious or life-threatening allergic reaction if they consume these products.
Bottles of the recalled Pat O’Brien’s Bloody Mary Cocktail Mix were distributed nationally in retail stores and through internet purveyors.
Price Chopper Supermarkets Issues Voluntary Cheesecake Recall
December 20, 2011 – Price Chopper Supermarkets is issuing a voluntary recall on the following three varieties of Price Chopper 24 oz. French Cheesecake from its bakery:
Raspberry with UPC 41735-22898
Blueberry with UPC 41735-22908
Strawberry with UPC 41735-22910
RECALL Green Valley Food Corp. “Let’s Grow Healthy Together!� Alfalfa Sprouts 5 oz. containers because of a possible health risk.
Green Valley Food Corp. of is recalling 650 cases of “Let’s Grow Healthy Together!� Alfalfa Sprouts 5 oz. containers, because the results showed to be contaminated with Salmonella, an organism that 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.
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McNeil Recall of Motrin IB Tablets and Caplets
McNeil Consumer Healthcare Division of McNEIL-PPC, Inc. (McNeil) is voluntarily recalling certain lots of MOTRIN® IB 24 count COATED CAPLETS, MOTRIN® IB 24 count COATED TABLETS and MOTRIN® IB 24+6 count COATED CAPLETS from retailers. The products were distributed in the United States, Puerto Rico, Bahamas, Fiji, Belize, St. Lucia and Jamaica.
FDA expands use of HIV drug Isentress to children and adolescents
Isentress (raltegravir) was approved today by the U.S. Food and Drug Administration for use with other antiretroviral drugs for the treatment of HIV-1 infection for children and adolescents ages 2-18.
FDA: Chicago-area sandwich manufacturer agrees to stop production
The U.S. Food and Drug Administration announced today that a Chicago-area company has agreed to stop making its ready-to-eat sandwiches and produce after FDA investigators repeatedly found unsanitary conditions and bacterial contamination in the facility.
Market Basket Initiates Limited Regional Voluntary Recall of Market Basket Solid White Albacore Tuna in Water 5 oz. Product Due to Undeclared Allergen
As a precautionary measure due to mislabeling, Market Basket is initiating a voluntary recall of its Market Basket Solid White Albacore Tuna in Water 5 oz. product — specifically, only those products with the Best Buy Dates of August 18, 2014 and August 19, 2014. Market Basket is voluntarily recalling this product because it contains vegetable broth, which contains soy, and soy is not declared as an allergen in the ingredient statement.
CareFusion Provides Update on Previously Announced Ventilator Recall
CareFusion issued the following update regarding the voluntary recall of AVEA® ventilators it initiated in September. The FDA has now classified this action as a Class I recall.