Posted by Editor
Wed, 19 Mar 2008 15:18:00 GMT
Food For Life Baking Company of Corona, California is voluntarily recalling 2,241 cases of Spelt Bread (UPC# 07347200168) because they contain spelt grain which is known to be a hybrid of wheat. People who have allergies to wheat or those with Celiac Disease may run the risk of a serious or life threatening allergic reaction if they consume spelt products.
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Posted in Food, Drugs & Medical Devices | Tags allergic reaction, allergies, baking company, bread food, celiac disease, corona ca, corona california, fda, fda investigation, food and drug, food and drug administration, food retailers, fruit juice, health food distributors, hybrid, illnesses, immediate release, natural food, precautionary measure, spelt products | no comments | no trackbacks
Posted by Editor
Mon, 10 Mar 2008 12:43:00 GMT
The Hartz Mountain Corporation is voluntarily recalling a second specific lot of Hartz Vitamin Care for Cats due to concerns that bottles within the lot may have been potentially contaminated with Salmonella. Hartz is fully cooperating with the US Food and Drug Administration in this voluntary recall. Hartz recalled a specific lot code of Hartz Vitamin Care for Cats last November due to similar concerns. Both lot codes were manufactured for Hartz by UFAC (USA) Inc. in 2007, and were removed from distribution last November. However, bottles from the second lot had been shipped to customers prior to their having been removed from distribution.
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Posted in Food, Drugs & Medical Devices | Tags abdominal pain, cat owners, diarrhea, food and drug administration, hartz mountain corporation, hartz products, health risk, immediate release march, last november, medical attention, nausea, organism, salmonella infection, salmonella symptoms, symptoms of salmonella, ufac, upc number, us food and drug administration, veterinary assistance, weakened immune systems | no comments | no trackbacks
Posted by Editor
Fri, 29 Feb 2008 18:33:00 GMT
Palo Alto Labs is conducting a voluntary nationwide recall of the company's supplement products sold under the name Aspire36 and Aspire Lite. Palo Alto Labs is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Aspire36 and Aspire Lite samples found that the products contained Aildenafil in trace amounts and Dimethyl sildenafil thione (sulfoaildenafil) a purported analog of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED).
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Posted in Food, Drugs & Medical Devices | Tags aspire36, blister pack, dangerous levels, dietary supplements, fda approved drug, food and drug administration, food and drug administration fda, high blood pressure, high cholesterol, medwatch program, nitrates, nitroglycerin, port st lucie, port st lucie fl, prescription drugs, sexual performance, supplement products, sw port st, thione, trace amounts | no comments | no trackbacks