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.
3,615 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Anzmtosn recalled 15-piece Magnet Fidget Spinner Sets sold on Amazon after magnets pose a serious ingestion hazard. The magnets can detach and, if swallowed, attract each other or metal objects and cause internal injuries. Stop using the sets now and email disposal photos to Anzmtosn53@163.com for a full refund.
Anna Queen recalls Play Yards sold on Amazon due to suffocation and entrapment risks. The product features black fabric sides, gray mesh panels, and white top rails with a bear-print design. Model P700 and production date 202503 appear on packaging and a removable tag. Consumers should stop using recalled units and obtain a full refund from Anna Queen.
Romorgniz recalled fabric 12- and 13-drawer dressers sold on Amazon after reports of tip-over and entrapment hazards. The units violate the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact Romorgniz for a full refund.
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.
A New Life Herbs, LLC recalled 144 bottles of Chaga Mushroom Herbal Supplement on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.
CareFusion 303 recalled 53,669 units of Automated Dispensing Cabinets on November 20, 2025. A firmware update caused drawer failures, leading to potential delays in accessing medications. This recall affects devices distributed worldwide, including all U.S. states and several countries.
Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.
A New Life Herbs recalled 48 bags of Organic Ginger Root Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume the product and seek a refund.
A New Life Herbs recalled 275 bottles of Pain Away Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume this product and seek refunds.
A New Life Herbs, LLC recalled 23 bottles of its Baby Allergy Herbal Supplement on November 20, 2025. The recall follows unapproved drug claims and absence of a Supplement Facts label on the product. Consumers should not consume the supplement and should seek refunds immediately.
Two Sonex aluminum pots sold in New York are recalled after tests found leachable lead at 0.323 mg/L. The recall is issued by Alanwar Food Corp. Consumers who own the pots should not use them for cooking and should contact Alanwar Food Corp. for refund or replacement information.
Vortex Surgical recalled 221 units of the 25ga Illuminated Flex-Tip Laser Probe on November 19, 2025. The product does not pass through a 25ga cannula smoothly, which poses a high hazard risk. Patients and healthcare providers must stop using the device immediately and follow recall instructions.
Steris recalled 22 AMSCO 7053HP Washer/Disinfectors on November 19, 2025, due to a risk of electrical arcing. The issue arises from a wire connected to the electrical box that may shift from its intended position. Users must stop using the device immediately and follow recall instructions.
Steris recalled the AMSCO 7052HP Washer/Disinfector on November 19, 2025, after reports of electrical arcing. The issue results from a wire potentially shifting out of position, posing a fire risk. No injuries or shocks have been reported.