Amneal Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Nizatidine Oral Solution, 15 mg/mL, Due to Potential Levels of N-nitrosodimethylamine (NDMA) Impurity Amounts Above the Levels Established by FDA

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Amneal Pharmaceuticals, LLC, Bridgewater, New Jersey is voluntarily recalling three lots of Nizatidine Oral Solution, 15 mg/mL (75 mg/5mL), packaged in 480 mL bottles to the Consumer Level. Nizatidine Oral Solution was distributed by Gemini Laboratories, LLC, a wholly owned subsidiary of Amneal Phar

Source: Food and Drugs Administration--Recalls/Safety Alerts

Avet Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Tetracycline HCl Capsules USP, 250 mg and 500 mg Due to Failed Dissolution Specifications

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Avet Pharmaceuticals Inc. (“Avet”), based in East Brunswick, New Jersey, is initiating a voluntary recall of the following lots of Tetracycline HCl Capsules USP, 250 mg and 500 mg, 100-count bottles listed in the table below to the consumer/user level. These drug products are manufactured by Avet Ph

Source: Food and Drugs Administration--Recalls/Safety Alerts

Avet Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Tetracycline HCl Capsules USP, 250 mg and 500 mg Due to Failed Dissolution Specifications

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Avet Pharmaceuticals Inc. (“Avet”), based in East Brunswick, New Jersey, is initiating a voluntary recall of the following lots of Tetracycline HCl Capsules USP, 250 mg and 500 mg, 100-count bottles listed in the table below to the consumer/user level. These drug products are manufactured by Avet Ph

Source: Food and Drugs Administration--Recalls/Safety Alerts

DSD Merchandisers, Inc. Issues Allergy Alert on Undeclared Peanut in Roasted/Salted Deluxe Mixed Nuts in Deli Tubs.

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DSD Merchandisers, Inc. of Livermore CA is recalling 2040 individual 10oz deli tubs of Roasted /Salted Deluxe Mixed Nuts, 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 con

Source: Food and Drugs Administration--Recalls/Safety Alerts

Allergy Alert Issued for Undeclared Milk in Minestrone Soup Sold at Whole Foods Market Stores in 32 States and the District of Columbia

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Whole Foods Market stores are voluntarily recalling Minestrone Soup because the products may contain undeclared milk.

Source: FDA Food Safety Recalls RSS Feed

Allergy Alert Issued for Undeclared Milk in Minestrone Soup Sold at Whole Foods Market Stores in 32 States and the District of Columbia

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Whole Foods Market stores are voluntarily recalling Minestrone Soup because the products may contain undeclared milk.

Source: FDA Food Safety Recalls RSS Feed

H&C Food Inc. Recalls Enoki Mushroom Because of Possible Health Risk

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H&C Food Inc. of Brooklyn, NY is recalling 7.05OZ (200G) Enoki mushrooms imported from Green Co. located in Korea, 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 peopl

Source: Food and Drugs Administration--Recalls/Safety Alerts

Viable Solutions, LLC Recalls Certain Kratom-Containing Powder Products Because of Possible Health Risk

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Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Source: FDA Food Safety Recalls RSS Feed

Homestead Creamery Recall “Unsalted” Butter Because of Possible Health Risk

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Homestead Creamery Inc of Wirtz, VA, is recalling our unsalted butter because of the potential contamination of 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.

Source: FDA Food Safety Recalls RSS Feed

Dr. Reddy’s Laboratories Issues Voluntary Nationwide Recall of Phytonadione Injectable Emulsion USP, 10 mg/mL Single-Dose Ampules Due To Ampules Breaking And Shattering Upon Opening

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Dr. Reddy’s Laboratories Ltd. (along with its subsidiaries together referred to as “Dr. Reddy’s”) announced today that it is voluntarily recalling four lots (ACB902, ACB903, ACB904, ACB905) of Phytonadione Injectable Emulsion USP, 10 mg/mL, Single-Dose Ampules to the hospital level. The product is b

Source: Food and Drugs Administration--Recalls/Safety Alerts