471 recalls tagged with “burn risk”.
Abbott Diabetes Care recalled 8,062 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may cause inaccurate low glucose readings, posing serious health risks. Consumers should stop using the device immediately and follow recall instructions.
Medline Industries recalled over 1.6 million oxygen masks on November 21, 2025. The recall affects multiple models after reports of tubing disconnecting during use. This defect can delay patient care and lead to shortness of breath, requiring medical intervention.
Demlar recalled MoonSoll ethanol and Magic Chems bioethanol fuel bottles sold online by the Demlar Online Store. The bottles lack flame mitigation devices required by the Portable Fuel Container Safety Act, creating a flash-fire risk. Consumers should stop using the recalled bottles immediately and contact Demlar for a full refund.
Mallimoda recalled its children’s pajama sets sold on Amazon due to a burn hazard risk. The recall cites violations of mandatory sleepwear standards. Consumers should stop using the recalled sets and contact Mallimoda for a full refund.
Molift recalled 71 Mover 300 mobile hoists on November 17, 2025, due to a potential bolt failure. The defect can lead to limited mobility, posing a high risk to users. Affected models include M1501, M1502, M1504, among others.
ETAC A/S recalled 25 units of the Molift 4-point sling bars on November 17, 2025, due to a defect that can lead to improper functionality. The issue stems from a bolt that may break during assembly and load testing, posing a high risk during use. This recall affects products distributed worldwide, including the United States and several European countries.
Tesla recalls Powerwall 2 energy storage systems sold through Tesla.com and certified installers nationwide due to fire and burn hazards. The lithium-ion cells can stop functioning during normal use, causing overheating and possibly smoke or flame. Owners should stop using the system and contact Tesla for replacement options.
Belkin is recalling its MMA008 charging stand and BPB002 and PB0003 power banks sold at multiple retailers due to a fire and burn hazard. The lithium-ion battery can overheat. Consumers should stop using the recalled devices immediately and contact Belkin for a full refund or store credit.
Jeni's Splendid Ice Creams recalls Passion Fruit Dreamsicle Ice Cream Bars for undeclared wheat and soy allergens. The recall covers 3,767 cases distributed to 10 states. Consumers should not eat the product and should seek a refund or replacement via email.
Zigjoy-US recalls Zigjoy-branded children's sleep sacks sold online after risk of serious burn injury. The recall covers blue sleep sacks with an excavator print and pink with a bunny print in sizes S, M, and L. The products claim 100% cotton on sewn-in labels. Consumers should stop using them immediately and seek a full refund.
Nissan North America recalls 2025 Kicks vehicles due to a Shift-to-Park warning that may not activate when the vehicle is shut off in a gear other than Park. The recall targets 2025 Nissan Kicks. Nissan will reconfigure the BCM to activate the warning at no cost. Notifications began January 29, 2025, with more letters expected May 7, 2025.
Olympus Corporation recalled 899 units of the Resection Sheath Model No. A42011A on November 11, 2025. Complaints indicate that the ceramic tip may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation recalled 29 units of its Resection Sheath on November 11, 2025. The recall affects model numbers A22014A and A22014T due to complaints of the ceramic tip breaking. The company advises immediate cessation of use and adherence to recall instructions.
Olympus Corporation of the Americas recalled 1,676 units of Resection Sheath Model No. A22042A on November 11, 2025. Complaints indicated the ceramic tip of the sheath could break during use, posing a hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled the Resection Sheath Model A2666T on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard for patients. Healthcare providers and patients should stop using the device immediately.
Olympus Corporation of the Americas recalled 1,634 units of the A22042T Resection Sheath on November 11, 2025. The recall follows complaints of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled 207 units of its Resection Sheath, Model No. A22043T, on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a serious hazard. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled 2,626 units of its Resection Sheath on November 11, 2025. The ceramic tip of the sheath may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.
Medline Industries recalled 163 DEXLOCK Achilles Repair Implant Kits on November 11, 2025, due to a potential hazard. Users reported drill bits fusing to the drill guide, which may prolong surgical procedures. The recall affects kits distributed nationwide in multiple states.
Olympus Corporation of the Americas recalled 7,426 units of the A22040T resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard to patients. Healthcare providers and patients must stop using the device immediately.