S&S Food Inc. at 1560 Troy Avenue, Brooklyn, NY 11203 is recalling DRIED FISH VOBLA GUTTED discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection and subsequent analysis of product by Food Laboratory personnel confirming that the fish was not properly eviscerated prior to processing.
This product may be contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food borne illness.
Rushing Waters Fisheries, Palmyra, is recalling about 225 pounds of smoked trout and smoked salmon
spreads, because the products may be contaminated with Listeria monocytogenes.
No illnesses have been reported from eating this product.
Lobby Shoppes, Inc. of Springfield, OH, is recalling the following three (3) products from distribution: Gourmet Cheese Popcorn in 12 oz. bags UPC Code 08299 11201 and 24 oz. bags; Chicago Triple Mix Popcorn in 12 oz. bags UPC Code 08299 11203; and (Delicious) Caramel Corn in 2 ½ lb. bags, 4 lb. bags, and 9 oz. tubs UPC Code 08299 11202. All recalled products are packaged in either clear plastic bags or clear plastic tubs.
Intelli Health Products announced today that it is expanding their voluntary nationwide recall of Duro Extend Capsules For Men, to include all lot codes. Intelli Health Products is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that laboratory analysis of Duro Extend Capsules For Men found the product to be adulterated with Sulfoaidenafil, an analogue of Sildenafil which is an FDA approved drug used in the treatment of Erectile Dysfunction (ED), making it an unapproved new drug.
In consultation with the U.S. Food and Drug Administration (FDA), Johnson & Johnson-Merck Consumer Pharmaceuticals, Co. (JJMCP) is recalling, from the wholesale and retail level, twelve MYLANTA® liquid products and one AlternaGEL® liquid product. JJMCP is conducting the recall in order to update the labeling for these products.
November 30 2010 — FDA today notified Wright County Egg LLC of Galt, Iowa, that the company has FDA’s concurrence to begin shipping shell eggs directly to the consumer market from two hen houses on one of its six farms. The firm has not shipped eggs to the consumer market since August 2010, when the company’s eggs were associated with the multi-state outbreak of Salmonella Enteritidis (SE). (DSK)
In response to a recall commenced by its supplier (Mincing Overseas Spice Company, Dayton, New Jersey), Frontier Natural Products Co-op, is voluntarily recalling two products manufactured with non-organic nutmeg that were sold under the Frontier brand and under the Whole Foods Market brand listed below that contain nutmeg supplied by Mincing Overseas Spice Company. The nutmeg has the potential to be contaminated with Salmonella.
Read The Complete Story!
McCormick & Company, Incorporated (NYSE:MKC) has announced a voluntary recall of Golden Dipt® Fry Easy All-Purpose Batter, 10 OZ, with UPC Code 4123470111 and “BEST BY” date of NOV 17 11 AH. A very limited number of packages of Golden Dipt® All-Purpose Batter with this date code contain an undeclared egg ingredient.
Read The Complete Story!
Marketed as a ’male sexual stimulant,’ product contains hidden drug ingredient
The U.S. Food and Drug Administration says Vigor-25, a product marketed as a natural dietary supplement to enhance male sexual performance, should not be purchased or used because it contains sildenafil, the active ingredient in the prescription drug Viagra.
Xanodyne Pharmaceuticals Inc. which makes Darvon and Darvocet, the brand version of the painkiller propoxyphene, has agreed to withdraw the medication from the U.S. market at the request of the U.S. Food Administration. The FDA has also informed generic manufacturers of Xanodyne’s decision and they will be removing their propoxyphene-containing products from the market as well.