Archive for the Food and Drug Category

Dash Xclusive Issues Voluntary Nationwide Recall of Imperia Elita Vitaccino Coffee Due to the Presence of Undeclared Sibutramine and Fluoxetine

May 11, 2021

Glendale, California, Dash Xclusive is voluntarily recalling all lots of Imperia Elita Vitaccino Coffee to the consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss bu Go to Source

Yamtun7 Issues Voluntary Nationwide Recall of Poseidon Platinum 3500 Due to the Presence of Undeclared Tadalafil and Sildenafil

May 10, 2021

Delray Beach, Florida, Yamtun7 is voluntarily recalling all lots of Poseidon Platinum 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil and sildenafil. Tadalafil and sildenafil are drugs known as phosphodiesterase (PDE-5) inhibitors found in FDA approved Go to Source

Natural Way Recalls Almond Butter Due to Undeclared Peanuts

May 6, 2021

Natural Way of Fayetteville, AR, is recalling its 16 ounce jars of original almond butter because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of a serious or life-threatening allergic reaction if they consume the product contained ins Go to Source

Arizona Nutritional Supplements Issues Allergy Alert on Undeclared Soy Allergen in 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor

May 6, 2021

Arizona Nutritional Supplements of Chandler, AZ is voluntarily recalling 13.9 oz. containers of “365 Everyday Value Whey Protein Powder Natural Vanilla Flavor” due to the potential of an undeclared soy allergen. Containers of 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor were mistak Go to Source

Novo Nordisk Issues Voluntary Nationwide Recall of Levemir®, Tresiba®, Fiasp®, Novolog® and Xultophy® Product Samples Due to Improper Storage Temperature Conditions

May 6, 2021

Novo Nordisk is voluntarily recalling 1,468 product samples listed in the table below of Levemir®, Tresiba®, Fiasp®, Novolog® and Xultophy®, to the consumer level. These products are being recalled because they were stored at temperatures below storage requirements. This recall only impacts product Go to Source

Revised Guan’s Mushroom Co Recalls Enoki Because of Possible Health Risk

May 5, 2021

Guan’s Mushroom Co of Commerce, CA is recalling all cases of its 100g/3.5- ounce & 200g/7-ounce packages of Enoki Mushroom (Product of China) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young child Go to Source

Bloommy, Inc Issues Allergy Alert on Undeclared Fish in Bloommy Biotin Collagen Keratin Capsules

May 5, 2021

Bloommy, Inc. is recalling the following product due to the presence of a fish allergen for the collagen-based ingredient. The best by involved or purchase date prior to 05/04/201.People who have an allergy or severe sensitivity to fish run the risk of serious or life-threatening allergic reaction i Go to Source

Frito-Lay Issues Voluntary Allergy Alert on Undeclared Milk In Ruffles All Dressed Potato Chips Distributed Regionally to Sam’s Club

May 4, 2021

Frito-Lay today issued a voluntary recall of select 16 1/8 oz. bags of Ruffles All Dressed Potato Chips because they may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the p Go to Source

Hershey Voluntarily Recalls Hershey’s Chocolate Shell Topping Due to Undeclared Almonds

May 4, 2021

The Hershey Company (Hershey) today announced a voluntary recall of a single lot of Hershey’s Chocolate Shell Topping in a 7.25-oz. (205g) bottle with UPC (346000) after learning that 1,700 bottles were incorrectly filled with Heath Shell Topping which is made with almonds. Hershey is initiating the Go to Source

Hospira Issues A Voluntary Nationwide Recall for One Lot of 0.5% Bupivacaine Hydrochloride Injection, USP and One Lot of 1% Lidocaine HCl Injection, USP Due to Mislabeling

May 3, 2021

Hospira, Inc., a Pfizer company, is voluntarily recalling lot EG6023 of 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and lot EG8933 of 1% Lidocaine HCl Injection, USP 30 mL, to the hospital/institution level due to mislabeling whereby a portion of each lot was incorrectly labeled as the other Go to Source

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