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.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
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 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.
EDAN recalled 3,518 fetal and maternal monitors on October 24, 2025, due to potential cybersecurity issues. Affected models include F6, F9, F6 Express, and F9 Express. The recall impacts devices distributed in the U.S. and Mexico.
EDAN recalled 14,550 Patient Monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The affected models include iM50, iM60, iM70, and iM80. Healthcare providers should stop using these devices immediately and follow the manufacturer's instructions for remedy.
EDAN recalled 377 iM20 Patient Monitors on October 24, 2025, due to cybersecurity issues. The recall affects devices distributed nationwide in the U.S. and Mexico. Healthcare providers must stop using this device immediately.
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.
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.
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.
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.
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.
Olympus Corporation of the Americas recalled 88,268 units of the Thunderbeat surgical device on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.
Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients must stop using this product immediately.
Olympus Corporation of the Americas recalled the Thunderbeat surgical device on October 22, 2025, due to reports of adverse events. The recall affects 30 units distributed worldwide, including the US, Canada, and Japan. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm Front-Actuated Grip on October 22, 2025. The recall follows ongoing reports of adverse events associated with the device. Healthcare providers and patients must stop using the instrument immediately.
Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 20 cm, Front-Actuated Grip on October 22, 2025. The recall follows ongoing reports of adverse events associated with the medical device. Patients and healthcare providers must stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 1,538 units of the Thunderbeat 5 mm, 10 cm, Inline Grip on October 22, 2025. The recall follows multiple reports of adverse events linked to the device. Healthcare providers and patients should stop using it immediately and follow the manufacturer's instructions.