471 recalls tagged with “burn risk”.
Medline Industries, LP recalled 1,928 circumcision procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which may crack during use. Healthcare providers and patients must stop using these kits immediately.
Sanven Technology recalled VEVOR Garment Steamers sold online after a burn hazard was identified. Affected units can leak or spit hot water, and the water tank cap can leak or detach. Consumers should stop using the recalled steamers and request a full refund from Sanven Technology.
Sanven Technology recalled Vevor ice crushers after a fire hazard was identified in BY-300 and BY-300 FS models. The units, sold as Ice Shavers, Ice Crushers and Snow Cone Makers, can experience a thermal event that could ignite. Stop using the recalled devices immediately and contact Sanven Technology for a full refund.
REPLIGEN Corporation recalled 33 Maverick Measurement Module Spectrometers on December 10, 2025. Disconnected or poorly crimped cables may cause elevated laser output or unintended firing. The recall affects devices distributed in the U.S.
Heraeus Medical GmbH recalled PALACOS R+G pro 40 and 80 bone cements on December 9, 2025. The recall follows multiple reports of ampoule breakage that prevent proper use of the product. Patients and healthcare providers must stop using the affected devices immediately.
Heraeus Medical GmbH recalled PALACOS MV+G pro 40 and MV+G pro 80 bone cement on December 9, 2025. The recall follows complaints about ampoule breakage, which can prevent proper cement formation. This issue could jeopardize patient safety during medical procedures.
Heraeus Medical GmbH recalled PALACOS MV pro 40 and MV pro 80 bone cement on December 9, 2025. The recall follows numerous complaints about ampoule breakage. This defect can prevent proper cement dough formation, rendering the product unusable for patients.
Intuitive Surgical recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.
Heraeus Medical GmbH recalled PALACOS R pro 40 and R pro 80 bone cement on December 9, 2025. The recall follows multiple complaints of ampoule breakage affecting product usability. Healthcare providers must stop using the product immediately.
Honda is recalling 2021-2025 Acura TLX, 2023-2025 Acura MDX, and 2023-2025 Honda Pilot vehicles over a brake pedal pivot pin that may loosen. The defect can shift the pedal, reducing braking ability. Dealer repairs are free. Honda notified owners on July 29, 2025. Contact Honda at 1-888-234-2138.
INIU recalled 10,000mAh portable power banks sold on Amazon after identifying a fire risk from overheating. The recall covers BI-B41 models with serial numbers 000G21, 000H21, 000I21 and 000L21. Consumers should stop using the recalled power banks immediately and contact INIU for a full refund.
Siemens Medical Solutions USA recalled LUMINOS Lotus Max and Luminos dRF Max systems on December 5, 2025. The recall affects systems with software version VF11 and involves a potential collimation error. Healthcare providers and patients must stop using the devices immediately.
Merit Medical Systems recalled multiple Custom Procedure Kits on December 4, 2025, due to a risk of the inflation device handle detaching from the syringe during use. The recall affects several reference numbers sold worldwide, including in the U.S. and various international markets.
Cubimana recalled treehouse building toy sets sold on Shein by Vatos Toys from July 2025 through October 2025. The recall list includes 618-piece sets and a LED light component containing a button cell battery. Parents should stop using the toy immediately and contact Vatos Toys for a full refund.
Merit Medical Systems recalled 864 units of its Custom Waste Management Kit Vascular Tray on December 4, 2025. The handle of the inflation device may detach from the syringe during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.
Primark US recalls Primark Water Balloon Pumps due to rupture risk. The affected units were sold at Primark stores in the United States from March 2023 through July 2023 for about $6. Consumers should stop using the pumps immediately and return them to a Primark store for a full refund.
Sysco Corporation recalled 17,597 cases of frozen potato product on December 3, 2025. The recall affects Sysco Imperial Potato Tater Barrel due to the presence of clear hard plastic fragments. Consumers should not consume this product and seek refunds immediately.
BMW of North America recalls 2025 X3 xDrive30 and X3 M50 xDrive after rear brake hoses may leak, causing a loss of rear brake function and disabling ABS and DSC. Owner notification letters were mailed May 9, 2025. If you own a 2025 X3 xDrive30 or X3 M50 xDrive, check your VIN now. Contact BMW customer service at 800-525-7417 for remedy details.
Zimmer, Inc. recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. These implants may have an undersized distal diameter that could lead to fatigue fractures. Patients should stop using the device immediately and contact their healthcare provider.
Zimmer, Inc. recalled 23 units of the Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, risking implant fatigue fracture. This defect can cause severe health issues, including pain and tissue damage requiring surgery.