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HUA SHING INTERNATIONAL TRADING CORP is recalling FROZEN SCDA (fish) 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 maybe contaminated with Clostridium botulinum spores, which can cause Botulism, a serious and potentially fatal food –borne illness.
Natural Choice Distribution Company Inc. is recalling certain ready-to-eat sandwiches and wraps because the products’ labels fail to declare food allergens. No illnesses have been reported. People who have allergies to MILK, WHEAT, SOY, OR EGGS run the risk of a serious or life-threatening allergic reaction if they consume these products.
Upsher-Smith Laboratories, Inc. is voluntarily expanding its previously announced recall of Jantoven® Warfarin Sodium, USP, 3 mg Tablets to include additional products that were packaged on the same packaging line between May 17, 2010 and November 17, 2010. The company is initiating the recall as a precautionary measure after a bottle labeled as Jantoven® Warfarin Sodium, USP, 3 mg Tablets was found by a retail pharmacy to contain tablets at a higher, 10 mg strength.
I've been slacking on this lately due to insane amounts of work... I also have several crazy stories from work that I haven't had/made time to write up for your entertainment. Sorry, I'll see what I can do about that around my 12 hour work days...
Natural Choice Distribution Company Inc. is recalling certain ready-to-eat sandwiches and wraps because the products’ labels fail to declare food allergens. No illnesses have been reported. People who have allergies to MILK, WHEAT, SOY, OR EGGS run the risk of a serious or life-threatening allergic reaction if they consume these products.
Upsher-Smith Laboratories, Inc. is voluntarily expanding its previously announced recall of Jantoven® Warfarin Sodium, USP, 3 mg Tablets to include additional products that were packaged on the same packaging line between May 17, 2010 and November 17, 2010. The company is initiating the recall as a precautionary measure after a bottle labeled as Jantoven® Warfarin Sodium, USP, 3 mg Tablets was found by a retail pharmacy to contain tablets at a higher, 10 mg strength.
I've been slacking on this lately due to insane amounts of work... I also have several crazy stories from work that I haven't had/made time to write up for your entertainment. Sorry, I'll see what I can do about that around my 12 hour work days...
