Innoveix Pharmaceuticals, Inc. Issues Voluntary Recall of All Sterile Compounded Drug Products Due to A Lack of Sterility Assurance

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Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots of sterile compounded drug products, within expiry. The products are being recalled due to a lack of assurance of sterility. These concerns arose following a routine inspection of the pharmacy by FDA.

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

LSG Sky Chefs Recalls Circle K Brand Chicken Salad Sandwich Because of Possible Health Risk

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LSG Sky Chefs announced today that it is issuing a voluntary recall of its Chicken Salad Sandwich 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 wit

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

LSG Sky Chefs Recalls Circle K Brand Chicken Salad Sandwich Because of Possible Health Risk

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LSG Sky Chefs announced today that it is issuing a voluntary recall of its Chicken Salad Sandwich 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 wit

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

Ardil Comercial Issues Voluntary Nationwide Recall of Limar Hand Sanitizer Packaged in 4 oz Bottles Because They Resemble Drink Containers

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Santo Domingo, Dominican Republic – Ardil Comercial is voluntarily recalling one lot of Limar Hand Sanitizer, packaged in 4 oz bottles to the consumer level. The hand sanitizer is being recalled because it is packaged in containers that resemble water bottles. The product poses a risk of ingestion

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

Teva Initiates Voluntary Nationwide Recall of One Lot of Topotecan Injection 4 mg/4 mL (1 mg/mL) Due to Presence of Particulate Matter

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Teva Pharmaceuticals has initiated a voluntary recall of lot 31328962B of Topotecan Injection 4 mg/4 mL (1 mg/mL), to the retail/institutional level in the United States. This voluntary recall was initiated based on a complaint received from a pharmacy after a single glass particle was observed ins

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

Manna Pro Products LLC Issues Limited Voluntary Recall of Flock Party Quack Snacks Sold in the United States Because of Possible Health Risk Due to Potential Salmonella Contamination

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Manna Pro Products, LLC, St. Louis, Missouri, is voluntarily recalling a single lot of Flock Party Quack Snacks (poultry treat) with a Best By date of 12/2023, packaged in 1.68 pound bags because it has the potential to be contaminated with Salmonella. Manna Pro Products LLC was informed by the Stat

Source: FDA Food Safety Recalls RSS Feed

Avanti Frozen Foods Recalls Frozen Cooked Shrimp Because of Possible Health Risk

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Avanti Frozen Foods Pvt. Ltd, with an abundance of caution, is recalling certain consignments of various sizes of frozen cooked, peeled, deveined, shrimp (with some packaged with cocktail sauce) sold in various unit sizes, because it has the potential to be contaminated with Salmonella. The frozen s

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

Dole Diversified North America, Inc. Announces Limited Recall of Dole™ Fresh Blueberries for Potential Cyclospora Contamination

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Dole Diversified North America, Inc. is recalling a limited number of cases of Dole™ Fresh Blueberries packaged in a variety of clamshell sizes for potential Cyclospora contamination.

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

Bazzini LLC Voluntarily Recalls Trader Joe’s Dark Chocolate Almond Butter Cup 2-Pak

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Bazzini LLC, Allentown, PA is, out of an abundance, voluntarily recalling three lot codes (SELL BY date codes of APR 05 2022, APR 06 2022, and APR 07 2022) of 1.4 ounce Trader Joe's Dark Chocolate Almond Butter Cups because it may contain peanut protein.

Source: FDA Food Safety Recalls RSS Feed

Bea Lydecker’s Naturals, Inc. Issues Allergy Alert on Undeclared Soy Lecithin in Living Free Dietary Supplement

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Bea Lydecker’s Naturals, Inc. of Oregon City, Oregon is recalling six Living Free brand dietary supplement products because labels declare lecithin but do not declare soy lecithin. People who have an allergy or severe sensitivity to soy should not consume these products.

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