burn risk Recalls

Zimmer Recalls Affixus Femoral Nailing System Over Fracture Risk

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.

Affixus Antegrade Femoral Nailing System Recalled Over Fatigue Risk

Zimmer Recalls Affixus Femoral Nails Due to Fracture 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 Recalls Affixus Antegrade Femoral Nails Over Fracture Risk

Zimmer issued a recall for 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized diameter, risking fatigue fractures. This defect could lead to severe health complications for patients.

Baxter Healthcare Recalls SIGMA Spectrum Infusion Pump Over Infusion Risk

RayStation Recalls Radiation Therapy System Over Dose Calculation Flaw

Medline Recalls Electric Homecare Beds Due to Fire Hazard

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.

Cook Medical Recalls Introducer Sheaths Over Manufacturing Errors

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Medline Recalls Homecare Beds Over Fire Risk from Hand Control

Ozark Trail Tabletop 1-Burner Butane Camping Stove BG2247A1 Recalled by Walmart in 2025

Medline Recalls Homecare Beds Over Fire Hazard Risk

Medline Recalls Electric Homecare Beds Due to Fire Hazard

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 Recalls IV Administration Sets Due to Valve Issues

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 Recalls IV Administration Sets Due to Valve Failure Risk

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 Recalls IV Administration Sets Due to Valve Malfunction

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.

Medline Recalls Homecare Beds Over Fire Hazard

Abbott Recalls FreeStyle Libre 3 Plus Sensors Due to Hazardous Readings

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Abbott Recalls FreeStyle Libre 3 Plus Sensor Over Glucose Errors

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Abbott Recalls FreeStyle Libre 3 Plus Sensors Over Low Glucose Risk

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Abbott Diabetes Care Recalls FreeStyle Libre 3 Sensor Over Glucose Reading Errors

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results