These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
1,488 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Draeger, Inc. recalled 431 units of the Vapor 2000 anesthetic vaporizer on November 24, 2025. A component of the devices contained impurities and did not meet specifications, posing a high hazard risk. Healthcare providers and patients should cease use immediately and follow recall instructions.
ICU Medical recalled the LifeShield Infusion Safety Software Suite v2.2 on November 24, 2025. The software fails to operate as expected for migrated libraries, risking medication delivery errors. The recall affects seven customers across several states, including California and New York.
ICU Medical recalled LifeShield Drug Library Management software on November 24, 2025. A software issue limits concentration precision to one decimal place, risking incorrect drug dosages. Users should stop using the product immediately and follow recall instructions.
Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.
Glenmark Pharmaceuticals recalled over 11,000 bottles of Bisoprolol Fumarate and Hydrochlorothiazide Tablets on November 21, 2025. Testing revealed traces of ezetimibe, posing a health risk. Consumers should stop using the product immediately and contact their healthcare provider.
Silvestri Sweets Inc recalled 37,314 bags of Choceur Pecan Cranberry & Cinnamon Holiday Bark on November 21, 2025. The recall stems from undeclared wheat, a serious allergen risk for consumers. The product was distributed nationwide through Aldi grocery stores.
Silvestri Sweets Inc recalled 37,314 bags of Cookie Butter Holiday Bark on November 21, 2025. The recall stems from undeclared pecan allergens, posing a risk to consumers with nut allergies. The affected product was distributed nationwide through Aldi stores.
Mallimoda recalled children's pajama sets on November 20, 2025, due to a serious burn hazard. The pajamas violate mandatory safety standards for children's sleepwear. Consumers should stop using them immediately and seek a refund.
Anna Queen recalled play yards on November 20, 2025, due to suffocation and entrapment hazards. The recalled model, P700, was sold exclusively on Amazon. Consumers should stop using these play yards immediately and seek a full refund.
Romorgniz recalled its Fabric 12- and 13-drawer dressers on November 20, 2025, due to a tip-over hazard. The dressers can pose serious injury or death risks to children if not anchored. Consumers should stop using the dressers immediately and seek a refund.
Bearlala recalled baby loungers on November 20, 2025, due to risks of serious injury or death from entrapment and falls. The loungers do not meet mandatory safety standards for infant sleep products. Consumers should stop using the loungers immediately and seek a refund.
Demlar recalled its MoonSoll and Magic Chems fuel bottles on November 20, 2025. The bottles pose a serious risk of flash fire due to missing safety features. Consumers should stop using them immediately and seek a refund.
Anzmtosn recalled its Magnet Fidget Spinner Sets on November 20, 2025, due to a serious ingestion hazard. The sets contain loose magnets that can pose a risk of severe injury or death to children. Consumers should stop using the product and seek a refund immediately.
Fagron Compounding Services recalled 2,980 syringes of a topical ophthalmic solution on November 20, 2025. The recall stems from an incorrect product formulation that could pose health risks. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
Doughy brand recalled 113 units of Chocolate Chip Cookie Dough on November 20, 2025. The product may be contaminated with Salmonella. Consumers should stop using the product immediately.
A New Life Herbs recalled 49 bottles of Baby Soothe Herbal Supplement on November 20, 2025. The product misbrands due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.
A New Life Herbs, LLC recalled 278 bottles of Boswellia Herbal Supplement on November 20, 2025. The product has unapproved drug claims and lacks a Supplement Facts label. Consumers should stop using it immediately and seek a refund.
A New Life Herbs, LLC recalled 22 bottles of Mullein flower alcohol tincture on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using this product immediately.
A New Life Herbs recalled Sinus Cap Herbal Supplement on November 20, 2025, due to unapproved drug claims. The product lacks a Supplement Facts label, which misbrands it. Consumers should not consume the product and seek refunds or replacements.
A New Life Herbs, LLC recalled 116 bottles of its anti-virus herbal supplement on November 20, 2025. The product misbranded due to unapproved drug claims and missing Supplement Facts label. Consumers should stop using the product immediately and seek a refund.