Western Milling announced today that it has voluntarily recalled 50 lb bags of Western Blend horse feed, LOT 5251, manufactured on September 8, 2015. This voluntary recall was initiated by Western Milling after it learned that an ingredient in the feed in question may contain monensin, an ionophore.
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FDA approves two new drug treatments for diabetes mellitus
The U.S. Food and Drug Administration today approved Tresiba (insulin degludec injection) and Ryzodeg 70/30 (insulin degludec/insulin aspart injection) to improve blood sugar (glucose) control in adults with diabetes mellitus.
Mr. Goodcents Franchise Systems, Inc. Voluntarily Issues Allergy Alert On Undeclared Peanuts In A Chocolate Chip Cookie
Mr. Goodcents Franchise Systems, Inc. of De Soto, KS is voluntarily recalling Chocolate Chip Cookies because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Mr. Goodcents Franchise Systems, Inc. Voluntarily Issues Allergy Alert On Undeclared Peanuts In A Chocolate Chip Cookie
Mr. Goodcents Franchise Systems, Inc. of De Soto, KS is voluntarily recalling Chocolate Chip Cookies because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Murphy Farm Hay and Feed Company Issues Recall of Alfalfa Hay Due to Possible Health Risk
Murphy Farm Hay and Feed Company of Louisburg North Carolina has initiated a voluntary limited recall of alfalfa hay due to potential Blister Beetle contamination. The product was offered for sale to consumers at the following two retail locations, Murphy Farm Hay and Feed in Louisburg, NC and Jones Farm Hay and Feed in Middlesex, NC.
Murphy Farm Hay and Feed Company Issues Recall of Alfalfa Hay Due to Possible Health Risk
Murphy Farm Hay and Feed Company of Louisburg North Carolina has initiated a voluntary limited recall of alfalfa hay due to potential Blister Beetle contamination. The product was offered for sale to consumers at the following two retail locations, Murphy Farm Hay and Feed in Louisburg, NC and Jones Farm Hay and Feed in Middlesex, NC.
Tastee Apple, Inc., Issues Allergy Alert On Undeclared Peanuts In Plain Caramel Apples
Tastee Apple, Inc., www.tasteeapple.com, issues allergy alert on undeclared peanuts in 3-ounce packages of Tastee Apples Plain Caramel Apples because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reactions if they consume these products.
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Greencore, USA – Rhode Island, Issues Allergy Alert Due to the Potential for Undeclared Almonds in Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola Parfaits Sold in 266 Locations in Massachusetts, Rhode Island, New Hampshire, New York, Connecticut, Vermont and Maine
Greencore, USA Inc. North Kingston, Rhode Island, is voluntarily recalling approximately 379 pounds (997 individual parfaits) of Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola parfaits because the product may contain undeclared almonds. People who have an allergy or sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume these products.
Lucy’s Weight Loss System Issues Voluntary Nationwide Recall of Pink Bikini and Shorts on The Beach Due to Undeclared Sibutramine and Phenolphthalein
Lucy’s Weight Loss System is voluntarily recalling all lots distributed May 25 – June 23 2015 of Pink Bikini and Shorts on the Beach Blue and Gold Edition, 30 blue capsules (750MG per) capsules and 30 gold capsule (800MG per) capsules to the consumer level. The Pink Bikini and Shorts on the Beach have been found positive for Sibutramine and Phenolphthalein after FDA sampling and testing.
US Compounding, Inc. Issues Voluntary Nationwide Recall of All Sterile Compounded Products
US Compounding, Inc. (“USC”) is voluntarily recalling all lots of sterile products aseptically compounded and packaged by USC and that remain within expiry due to the Food and Drug Administration’s (“FDA”)_ concern over a lack of sterility assurance. The sterile products were distributed nationwide to patients, providers, hospitals, or clinics between March 14, 2015 and September 9, 2015.