Medline Industries, LP Issues Nationwide Recall of SubG Endotracheal Tube with Subglottic Suction

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On February 20, 2024, Medline Industries, LP initiated a nationwide recall of 6 SubG Endotracheal Tubes with Subglottic Suction and 10 kits that contain these devices. The inflation tube and other device components have become detached and/or torn from the main tube, resulting in moisture buildup, l

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

Fresh Start Produce Sales Initiates Recall of Whole Cucumbers Because of Possible Health Risk

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Fresh Start Produce Sales Inc. of Delray, Florida, is recalling whole cucumbers shipped to certain states from May 17th through May 21st, 2024, due to the potential to be contaminated with Salmonella, an organism that can cause serious and sometimes fatal infections in young children, frail or elder

Source: FDA Food Safety Recalls RSS Feed

Heinen’s Issues Allergy Alert on Undeclared Pecans in Heinen’s Tuscan Salad Bowls

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May 30th, 2024. Heinen’s of Warrensville Heights, OH is voluntarily recalling Heinen’s Tuscan Salad Bowls, due to the possibility that it may contain undeclared Pecans. While no reports of injury have occurred, out of an abundance of caution people who have an allergy or severe sensitivity to Pecans

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

Sagent Pharmaceuticals Issues Voluntary Nationwide Recall of Docetaxel Injection, USP Due to Potential Presence of Particulate Matter

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Sagent Pharmaceuticals today announced the voluntary nationwide recall of two lots of Docetaxel Injection, USP (80 mg per 8 mL multi-dose vials and 160 mg per 16 mL multi-dose vials). The product was distributed by Sagent Pharmaceuticals. Sagent has initiated this voluntary recall of Docetaxel Injec

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

Dairy Manufacturers Inc. Issues Voluntary Recall of Products Due to Non-Compliance with Requirements Under the 21 CFR 106.110 New Infant Formula Registration

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Dairy Manufacturers Inc., of Prosper, TX – 5/24/24, is voluntarily recalling all lot codes for infant formulas available in the US: Crecelac Infant 0-12, Farmalac 0-12 and Farmalac 0-12 Low lactose to the retail and wholesale level. The products have been found in non-compliance with the requirement

Source: FDA Food Safety Recalls RSS Feed

AMB Food Inc. Issues Allergy Alert on Undeclared Wheat in Product

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AMB Food Inc. in Brooklyn NY is recalling 8 oz bags of Pop a Nosh Mix Munch Regular and Honey BBQ snacks because it contains pretzels, but does not list Wheat as an allergen. People who have an allergy or severe sensitivity to wheat run the risk of serious or life-threatening allergic reaction if th

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

World Green Nutrition, Inc. Expands Recall of Tejocote Products Due to the Presence of Yellow Oleander

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World Green Nutrition, Inc is announcing the expansion of their April 03, 2024 recall to include more lot numbers of the products GREEN ELV NUTRITION brand Elv Control Herbal Supplement 90 capsules and ELV ALIPOTEC brand Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento e

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

County Road Seafood Issues Allergy Alert of Undeclared Egg in 4 Oz Packages of County Road Seafood Crab Cake

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County Road Seafood, LLC., of Belhaven, NC – May 21, 2024, is voluntarily recalling County Road Seafood Crab Cake 2 Pack 4 Ounce package because this product contains undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction

Source: FDA Food Safety Recalls RSS Feed

Hospira Inc. Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units Due to the Potential for Incomplete Crimp Seals

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Hospira, Inc., a Pfizer company (“Pfizer”), is voluntarily recalling the lots listed in the table below of Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units to the User level. The recall was initiated due to the potential for incompl

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

Reser’s Fine Foods Announces Voluntary Recall of Single Batch of Aldi Macaroni 32 oz Salad with Use By Date of Jun/03/24 Due to Unlabeled Wheat Allergen

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Reser’s Fine Foods is voluntarily recalling a single item with a specific use by date, produced at a regional facility and distributed to ALDI. The product is the Aldi Deli Macaroni Salad 32 oz, with a Use By Date of Jun/03/24 due to an incorrect label. The incorrect label does not include an all

Source: FDA Food Safety Recalls RSS Feed