Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Siemens Medical Solutions USA recalled one MAMMOMAT Fusion operator table on October 24, 2025. The table was sold with a bus-installation kit but is intended for stationary use only. This recall affects distribution in Arkansas, California, New York, and internationally in Australia, Canada, and India.
Water Pure recalled 17,612 bottles of My Bladder dietary supplement on October 24, 2025. The product may be contaminated with E. coli O7:K1 and E. coli 1303. Consumers should stop use immediately and seek refunds.
GE Medical Systems recalled 1,818 Senographe Pristina mammography systems on October 24, 2025. The recall affects systems due to missing or incorrect X-Ray Warning labels. This nonconformance to FDA regulations poses a high hazard risk.
Invagen Pharmaceuticals recalled Lanthanum Carbonate chewable tablets on October 24, 2025, due to stability issues. The tablets failed hardness specifications, posing a high hazard level. Healthcare providers and consumers should stop using the product immediately.
Cipla USA recalled 1,180 boxes of Lanthanum Carbonate chewable tablets on October 24, 2025. The recall follows a failure to meet stability specifications for hardness tests. Consumers and healthcare providers must stop using the product immediately.
Bealife recalled 5,000 dressers on October 23, 2025, due to significant tip-over risks. The dressers can cause serious injuries or fatalities if not anchored to a wall. The recall involves model number AP23-W, which is only printed on the packaging.
3M Company recalled the Scotch™ Thermal Laminator model TL909-50 on October 23, 2025. The laminator can overheat, posing a burn hazard. Consumers are urged to stop using the product immediately.
Lifepro Fitness recalled Bioremedy Infrared Sauna Blankets on October 23, 2025, due to burn hazards. The recall affects all models with a gray-faced control pad. Consumers should stop using the blankets immediately.
LEACHOI recalled its adult portable bed rails on October 23, 2025, due to serious entrapment and asphyxiation hazards. The recalled product violates mandatory safety standards for bed rails and poses a high risk of injury or death. Consumers should stop using the bed rails immediately and seek a full refund.
Sauna360 recalled Tylö Halmstad and Kiruna Hybrid saunas on October 23, 2025, due to a fall hazard. The recalled products include models with potential bench collapse issues. Consumers should stop using the saunas immediately and contact the manufacturer for repairs.
Scepter recalled fuel containers on October 23, 2025, due to serious fire risks. The recall affects containers that lack safety features required by law. Consumers should stop using these products immediately and seek a refund.
Cranach Hardware recalled defective tip restraint kits on October 23, 2025. The plastic components can degrade and fail to secure furniture, posing a serious tip-over risk. Young children and elderly adults are at risk of severe injuries from tipping furniture.
Olympia Tools International recalled its Pack-N-Stroll Premium Folding Utility Wagons on October 23, 2025. The wagons pose a risk of serious injury or death from entrapment and falls. Consumers should stop using them immediately and return to Costco for a full refund.
J & D Brush recalled Bio Ionic One-Inch-Long Barrel Curling Irons on October 23, 2025. The curling irons may snap, posing a burn risk. Consumers should stop using the product immediately and seek a replacement.
Scepter recalled fuel containers on October 23, 2025, due to fire and poisoning risks. The containers lack required safety features, posing a high hazard. Consumers must stop using them immediately and seek refunds.
Bristol-Myers Squibb recalled 12,778 vials of Opdualag injection on October 21, 2025. The recall stems from a lack of assurance of sterility. The affected products were distributed nationwide in the United States.
Medtronic MiniMed recalled 12,126 glucose monitoring devices on October 21, 2025. A software error can lead to incorrect glucose readings, risking hypoglycemia or hyperglycemia. Affected consumers should stop using the device immediately and contact their healthcare provider.
Mindray DS USA, Inc. recalled 148 units of the V90 Electronic Vaporizer on October 20, 2025. The recall follows reports of potential anesthesia leakage that could impact patient safety. Healthcare providers and patients must stop using the device immediately.
Mindray DS USA, Inc. recalled 54 units of the Isoflurane V90 Electronic Vaporizer on October 20, 2025. The recall stems from a potential anesthesia leakage issue that poses serious health risks. Affected devices were distributed in the U.S. and Canada.
Straumann USA recalled 61 units of Emdogain on October 17, 2025. The product, intended for demonstration only, poses a risk if used on patients. Consumers must stop using the affected products immediately.