electrical hazard Recalls

GE Healthcare Omni Legend Recalled Due to Image Artifact Risk

Focalyx Technologies Recalls Software Device Over Patient Safety Risks

Medline Electrophysiology Catheters Recalled Over Infection Risk

Medline ReNewal Catheters Recalled Due to Infection Risk

Medline Industries Issues Recall of Catheters Over Infection Risk

Medline Recalls St. Jude Electrophysiology Catheters Over Infection Risk

Medline Industries recalled reprocessed St. Jude electrophysiology catheters on December 22, 2025. The recall affects 48 units potentially contaminated with residual materials. The defective catheters pose a high risk of inflammation and systemic infection.

LSL Healthcare Recalls Central Line Dressing Kits Due to Seal Failure

LSL Healthcare recalled 1,400 Central Line Dressing Kits on December 22, 2025. BD ChloraPrep Triple Swabsticks in these kits have open seals on their packaging. This defect poses a serious risk during medical procedures.

Abbott Catheters Recalled Over Risk of Infection and Embolism

Abbott recalled reprocessed steerable diagnostic catheters on December 22, 2025, after discovering potential contamination. The devices may contain small particles that pose risks of systemic infection or embolism. A total of 311 units are affected nationwide.

Medline Catheters Recalled Over Infection Risk

Altruan GmbH Bisaf Strep A Self-Test Recalled for FDA Clearance Issue

Product not cleared by the FDA.

Boston Scientific Stent Recalled Over Deployment Issues

Boston Scientific recalled 59 AXIOS Stents on December 19, 2025. Increased reports of deployment and expansion issues pose serious risks during procedures. Users should stop using the devices immediately and follow recall instructions.

Canon Medical Recalls Alphenix INFX-8000C X-Ray System Over Safety Risk

Tyber Medical Recalls VOLT Wrist Treatment System Due to Hazard

The supplier manufactured anatomical left plates with an incorrect thread orientation.

Canon Medical Recalls MRI Systems Over High-Pressure Hazard

Boston Scientific Recalls HOT AXIOS Stent Over Deployment Issues

ICU Medical Recalls Pulsator Arterial Blood Sampling Kit for Hazard

ICU Medical recalled 64,290 Pulsator Arterial Blood Sampling Kits due to a potential crack in the syringe collar. This defect may cause blood leakage and delayed sampling. The recall affects models sold nationwide since December 2025.

Tornier Recalls Surgical Screws Over Labeling Error

ICU Medical Recalls Needles Free Access Devices Due to High Risk of Leakage

ICU Medical Recalls Spinal Tray Syringes Due to Leakage Risk

Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.

Siemens Medical Recalls NAEOTOM Alpha CT Software Over FDA Clearance Issue

To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.