Bonduelle USA Inc. of Brockport, NY is recalling 9,335 cases of frozen corn because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
VRVK Nutraceuticals, LLC Issues Allergy Alert On Undeclared Crustacean Shellfish And Milk In Two Lots Of Ultimate Antioxidant Tablets
VRVK Nutraceuticals, LLC, DBA DR. VENESSA’S FORMULAS of Orlando, Florida, is voluntarily recalling 3998 bottles of ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, with Kelp Atlantic Powder that may contain crustacean shellfish, an undeclared allergen. This product also contains Hesperidin Complex 40%, Pancreatin Powder and Pepsin, three ingredients that contain undeclared milk.
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VRVK Nutraceuticals, LLC Issues Allergy Alert on Undeclared Crustacean Shellfish and Milk in Two Lots of Ultimate Antioxidant Tablets
VRVK Nutraceuticals, LLC, DBA DR. VENESSA’S FORMULAS of Orlando, Florida, is voluntarily recalling 3998 bottles of ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT, 120 count bottles, with Kelp Atlantic Powder that may contain crustacean shellfish, an undeclared allergen. This product also contains Hesperidin Complex 40%, Pancreatin Powder and Pepsin, three ingredients that contain undeclared milk.
Tasty Delicious Bakery Inc. Issues Allergy Alert On Undeclared Eggs In Sugar Bun
TASTY DELICIOUS BAKERY INC.of Brooklyn, New York is recalling Sugar Bun in 8 oz individually wrapped packages because it may contain eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
Insulet Corporation Issues Voluntary Recall of OmniPod Insulin Management System
On July 8, 2015, Insulet Corporation (Insulet or the Company) initiated a lot-specific voluntary recall of 40,846 boxes (10 Pods per box) of the OmniPod (Pod) Insulin Management System. This field corrective action is due to the possibility that some of the Pods from these lots may have a higher rate of failure than Insulet’s current manufacturing standards.
FDA approves Repatha to treat certain patients with high cholesterol
The U.S. Food and Drug Administration today approved Repatha (evolocumab) injection for some patients who are unable to get their low-density lipoprotein (LDL) cholesterol under control with current treatment options.
The One Minute Miracle Inc. Issues Voluntary Nationwide Recall of MIRACLE DIET 30 Due to Presence of Undeclared Phenolphthalein & MIRACLE ROCK 48 Due to Presence of Undeclared Thiosildenafil
The One Minute Miracle Inc. is voluntarily recalling one lot each of Miracle Diet 30, capsules and Miracle Rock 48.
Miracle Diet 30 has been found to contain undeclared phenolphthalein, phenolphthalein was an ingredient used in over-the counter laxatives but was removed from the market because of concerns of carcinogenicity.
Bimbo Bakeries Voluntary Regional Recall of Certain Limited Breads Produced Under the Sara Lee, Great Value, Kroger, Bimbo, Nature’s Harvest and L’Oven Fresh Brands
Bimbo Bakeries USA has initiated a voluntary regional recall of certain bread products under the Sara Lee®, Kroger®, Bimbo®, Nature’s Harvest®, Great Value and L’Oven Fresh® brands due to the possible presence of fragments of glass caused by a broken light bulb at one of its bakeries.
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FDA takes action against three tobacco manufacturers for making “additive-free” and/or “natural” claims on cigarette labeling
Today the U.S. Food and Drug Administration issued warning letters to three tobacco manufacturers — ITG Brands LLC, Santa Fe Natural Tobacco Company Inc., and Sherman’s 1400 Broadway N.Y.C. Ltd. — who describe their cigarettes on product labeling as “additive-free” and/or “natural.” The warning letters are for violations of section 911 of the Federal Food, Drug, and Cosmetic Act (FD&C Act).
General Mills voluntarily recalls a limited quantity of frozen Cascadian Farm Cut Green Beans
General Mills today announced a voluntary Class I recall of a limited quantity of frozen Cascadian Farm Cut Green Beans produced over two days in March 2014. The recall is being issued as a precaution after one package of finished product tested positive for the presence of Listeria monocytogenes.