425 recalls tagged with “burn risk”.
Zimmer Inc. recalled 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have undersized distal diameters, risking implant fatigue fractures. Consumers should stop using the device immediately and follow manufacturer instructions.
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 recalled 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, risking fatigue fractures. This can lead to serious health complications requiring surgical intervention.
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.
RaySearch Laboratories AB recalled its RayStation/RayPlan system on November 28, 2025. The recall affects software version RayStation 10B SP1, citing a high-risk hazard in radiation dose calculations. Affected systems may not invalidate doses as intended for certain Regions of Interest.
Baxter Healthcare recalled 585 SIGMA Spectrum Infusion Pumps on November 28, 2025, due to a defect that may cause over-infusion. The affected model is the 35700BAX2, which has been distributed nationwide. Users must stop using the device immediately and follow recall instructions.
Medline Industries recalled 3,045 IV administration kits on November 26, 2025. The recall affects several Medline kits due to potential malfunction of check valve components. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 1,725 IV Administration Sets on November 26, 2025. The recall affects multiple kits due to potential valve malfunctions. Consumers and healthcare providers must stop using these devices immediately.
Medline Industries recalled 12 IV administration kits on November 26, 2025. The kits may contain defective check valve components that can become stuck. Patients and healthcare providers should stop using these devices immediately.
McLee Creations recalled MyOnlyStyler Root Booster Hair Dryers on November 26, 2025, due to electrocution hazards. The recalled model, MOS-22, was sold in white with black bristles. Consumers should stop using the product immediately and return it for a refund.
Walmart recalled Ozark Trail Tabletop 1-Burner Butane Camping Stoves on November 26, 2025. The stoves pose serious burn and fire hazards due to possible explosions. Consumers should stop using the product immediately and return it for a full refund.
Cook Medical recalled 7,952 Flexor Check-Flo introducers and sets on November 26, 2025. The devices may have been manufactured out of specification, potentially posing serious risks to patients. Health care providers and patients should stop using these products immediately.
Medline Industries recalled 13,245 homecare beds on November 26, 2025, due to a fire risk from the hand control pendant. The company received 58 reports of sparking, burning, and smoke. Patients and healthcare providers must stop using the beds immediately and follow recall instructions.
Medline Industries recalled 15,581 electric homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat, posing a risk of fire in rare cases. The recall follows 58 complaints of sparking or burning from the pendant.
Medline Industries recalled 138,412 electric homecare beds on November 26, 2025. Hazardous hand control pendants may overheat and pose a fire risk. The recall follows 58 reports of sparking, burning, and smoking incidents.
Medline Industries recalled 35,694 Full Electric Lightweight Homecare Beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat under certain conditions, leading to potential fire risks. The company received 58 complaints related to sparking and burning incidents.
Medline Industries recalled 22,565 Full Electric Low Basic Homecare Beds on November 26, 2025, due to a fire risk. The recall affects beds labeled with REF MDR107003ELO following 58 reports of overheating hand control pendants. Consumers should stop using the beds and follow recall instructions immediately.
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.
Abbott Diabetes Care recalled 1,663,241 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may lead to incorrect low glucose results, creating serious health risks for users. Patients should stop using the sensors immediately and follow recall instructions.
Abbott Diabetes Care recalled 258,913 FreeStyle Libre 3 Plus sensors on November 24, 2025. Manufacturing issues may lead to incorrect low glucose results, posing a high risk to users. Consumers should stop using the device immediately and follow the recall instructions.