425 recalls tagged with “burn risk”.
Nipro Medical Corporation recalled the Surdial DX Hemodialysis System on October 27, 2025, after reports of screws loosening and potentially falling out. The recall affects devices distributed nationwide across 19 states. Patients and healthcare providers must stop using the device immediately and follow manufacturer guidance.
Medline Industries recalled 18,000 units of Curad Quick Strip Fabric Bandages on October 27, 2025. The recall affects all lots due to compromised seals that may affect sterility. Consumers should stop using these bandages 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.
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.
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.
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.
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 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.
Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm, Pistol Grip device on October 22, 2025. The recall affects 30 units distributed worldwide, including the U.S., Canada, Brazil, Germany, Mexico, and Japan. Patients and healthcare providers must stop using this device immediately due to reports of adverse events.
Olympus Corporation of the Americas recalled 140 units of its Thunderbeat surgical device on October 22, 2025. Users reported ongoing adverse events linked to the device. Healthcare providers should stop using it immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 52 units of the Thunderbeat, 5 mm, 35 cm, Inline Grip on October 22, 2025. Reports of adverse events prompted the removal of this medical device from the market. The recall affects distribution in the US, Brazil, Canada, Germany, Mexico, and Japan.
Olympus Corporation of the Americas recalled 4,181 units of its Thunderbeat surgical device on October 22, 2025. Reports of adverse events prompted the removal of this device. The recall affects devices distributed worldwide, including the US, Brazil, Canada, Germany, Mexico, and Japan.
Olympus Corporation recalled 3,381 units of the Thunderbeat surgical instrument on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using the product 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 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, 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.
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.
Town Food Service EQ CO Inc. recalled approximately 11,300 aluminum sauce pans on October 17, 2025, due to leachable lead levels. Consumers should not use these pans and should seek refunds or replacements. The recall affects various sizes sold across multiple states and locations in Canada.