Fresh Express Incorporated is voluntarily recalling a limited quantity of expired 18 oz. Hearts of Romaine salad with the expired Use-by Date of September 26, 2012 and Product Code H256808 as a precaution due to a possible health risk. No consumer complaints have been received by Fresh Express Consumer Response Center in association with this … [Read more...]
Stryker Issues Class 1 Recall of Neptune Rover Waste Management System in the United States, Asia Pacific, Canada, Japan, Latin America and EMEA
Contact: Consumer: 269-389-2316 or strykerinstrumentsrecalls@stryker.com FOR IMMEDIATE RELEASE September 25, 2012 - On June 5, 2012, Stryker initiated a Class 1 recall of the Neptune Waste Management System. The devices are being recalled because Stryker has received two reports of serious injury as a result of tissue damage associated with the use … [Read more...]
Evol Nutrition Associates, Inc./ Red Dawn Issues Voluntary Nationwide Recall of DietarySupplements Mojo Nights and Mojo Nights for Her Because of Potential Health Risk
Kennesaw, GA, Evol Nutrition Associates, Inc./Red Dawn ("Evol Nutrition") announced today that it is conducting a voluntary nationwide recall of all lots of two dietary supplement products distributed by the company under the names Mojo Nights and Mojo Nights for Her to the consumer level. The products are manufactured by and are products of Mojo … [Read more...]
Del Monte Fresh Produce N.A. Inc, Recalls Limited Quantity of Fresh-Cut Mango Products Due to Possible Health Risk – This Recall is Associated with FoodSource’s recall of Mangoes Sourced from Agricola Daniella In Mexico
In cooperation with the FDA's warning to not consume mangoes from Agricola Daniella in Mexico, Del Monte Fresh Produce N.A., Inc, is initiating a voluntary recall of 1,600 bowls of fresh-cut mangoes distributed to retail outlets due to the potential risk that the mangoes may contain Salmonella. Salmonella is an organism which can cause serious and … [Read more...]
Watson Issues Voluntary Nationwide Recall of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg Due to the Potential for Oversized and Superpotent Tablets
WatsonLaboratories, Inc. today issued a voluntary nationwide recall for two lots of Hydrocodone Bitartrate and APAP Tablets, USP 10 mg/500 mg. A customer complaint was received for tablets that were thicker and darker shade than the other tablets. It is possible that some tablets from lots 519406A and 521759A exceed the weight specification and may … [Read more...]
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