Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
EDAN recalled 3,721 fetal monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The affected models, F2 and F3, are used to monitor pregnant women and fetuses after 28 weeks of gestation. Healthcare providers must stop using these devices immediately and follow recall instructions.
Siemens Medical Solutions USA recalled six MAMMOMAT Inspiration operator tables on October 24, 2025. The operator tables were sold with a bus-installation kit, which they are not designed for. This recall affects three units in the U.S. and three internationally.
EDAN recalled 136 vital signs monitors on October 24, 2025, due to potential cybersecurity issues. The devices include models iM3s, iM3As, iM3Bs, and iHM3s. Patients and healthcare providers must stop using these monitors immediately and follow recall instructions.
EDAN recalled 395 units of its Central Monitoring System on October 24, 2025, due to potential cybersecurity risks. The affected models include MFM-CNS and MFM-CNS Lite, which manage critical fetal and maternal health data. Healthcare providers must stop using the devices immediately and follow the recall instructions.
EDAN recalled 342 patient monitors on October 24, 2025, due to potential cybersecurity issues. Models affected include elite V5, elite V6, and elite V8. Healthcare providers and patients should stop using these devices immediately.
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.
EDAN recalled 354 units of its M3B Vital Signs Monitor on October 24, 2025, due to potential cybersecurity vulnerabilities. The recall affects devices distributed nationwide in the U.S. and Mexico. Patients and healthcare providers should stop using the device immediately and follow the manufacturer's instructions for returning the product.
MeriCal, LLC recalled 698,064 units of its Super Greens Dietary Supplement on October 24, 2025. The recall follows potential contamination with Salmonella Richmond. Consumers should not consume the product and seek refunds immediately.
EDAN recalled 379 patient monitors on October 24, 2025, due to potential cybersecurity issues. Models iX10, iX12, and iX15 pose risks to patient safety. Healthcare providers should stop using these devices immediately.
EDAN recalled 1,457 iT20 telemetry transmitters on October 24, 2025, due to potential cybersecurity issues. The recall affects devices distributed in the United States and Mexico. Healthcare providers and patients must immediately discontinue use of the device.
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.
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.
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.
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.
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.
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.