Humei Trading Inc of 147-34 176th Street 1st Floor, Jamaica NY 11434, is recalling its 340g (12oz) Packages of “Dried Lily” because they contained undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
K-Fat Inc. Issues an Alert on Undeclared Sulfites In Kfi Sweetened Ginger Cand
K-Fat Inc. 13 Meadow St. Brooklyn, N.Y., 11206 is recalling KFI Sweetened Ginger Candy because they contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
FDA approves pediatric use of Dexcom’s G4 Platinum continuous glucose monitoring system
The U.S. Food and Drug Administration today approved the expanded use of the Dexcom G4 Platinum Continuous Monitoring System for patients with diabetes ages 2 to 17 years. The G4 Platinum System, which monitors blood glucose levels in people with diabetes, had been approved for patients ages 18 and older.
UPDATE: Unified Grocers, Inc. Issues Allergy Alert on Undeclared Eggs in “Special Value Ginger Snap Cookies”
Unified Grocers is recalling its 12 ounce bags of “Special Value Ginger Snap Cookies” because they may contain undeclared eggs. People who have allergies to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
FDA Approves Hetlioz: first treatment for non-24 hour sleep-wake disorder in blind individuals
The U.S. Food and Drug Administration today approved Hetlioz (tasimelteon), a melatonin receptor agonist, to treat non-24- hour sleep-wake disorder (“non-24”) in totally blind individuals. Non-24 is a chronic circadian rhythm (body clock) disorder in the blind that causes problems with the timing of sleep. This is the first FDA approval of a treatment for the disorder.
FDA proposes rule to prevent food safety risks during transportation
The U.S. Food and Drug Administration today proposed a rule that would require certain shippers, receivers, and carriers who transport food by motor or rail vehicles to take steps to prevent the contamination of human and animal food during transportation.
YoungYou International Issues Voluntary Recall of Mega Slim Herbal Appetite Management Pills Due to Presence of DMAA
YoungYou International (“YoungYou”) is voluntarily recalling Mega Slim Herbal Appetite Management, one pill a day, sold from September 15, 2013 through January 23, 2014 at the consumer level. Mega Slim Herbal Appetite Management was found to contain DMAA.
Gano Excel USA Inc. Announces Recall of C’Real Spirulina
Gano Excel USA, Inc. of Irwindale, CA is recalling all C’Real Spirulina. C’Real Spirulina is being recalled because of the undeclared food allergens, wheat and soy. People who have allergy or severe sensitivity to wheat and/or soy run the risk of life threatening allergic reaction, anaphylaxis, that requires immediate medical care if they consume the product.
FDA Statement on Western Sugar Cooperative voluntary recall of beet pulp and tailings
he U.S. Food and Drug Administration, in close coordination with the Wyoming Department of Agriculture (WDA) and the U.S. Department of Agriculture (USDA), has been working to address a tragic accident that occurred at the Western Sugar Cooperative’s Lovell, Wyo., manufacturing facility on Jan. 4, 2014.
Pringles Issues Allergy Alert and Voluntary Recall of One Hour’s Worth of Production of Original Crisps Due to Undeclared Milk
Pringles is recalling a small quantity of 5.68‐ounce cans of its Original crisps. The crisps are being recalled because they may have been inadvertently exposed to seasoning containing milk, which is not listed as an ingredient on the label.
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