Health & Personal Care Recalls

Medline Industries Recalls Ultrasound Catheters Over Infection Risk

Medline Electrophysiology Catheters Recalled 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.

DPT Laboratories Recalls Diclofenac Sodium Gel Over PH Specification Failure

Medline Catheters Recalled Over Infection Risk

Boston Scientific Issues Recall for Stent Due to Deployment Issues

Boston Scientific recalled 588 units of its *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System on December 19, 2025. The recall follows multiple reports of stent deployment and expansion issues, posing serious risks during medical procedures.

Boston Scientific Recalls AXIOS Stent Over Deployment Issues

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.

Boston Scientific Recalls Stent System Due to Deployment Issues

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

Product not cleared by the FDA.

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.

Boston Scientific Recalls HOT AXIOS Stent Over Deployment Issues

Tyber Medical Recalls VOLT Wrist Treatment System Due to Hazard

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

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

Canon Medical System Recalls Interventional X-Ray Systems Over Safety Risk

Siemens Medical Recalls CT Software Over FDA Clearance Issues

Siemens Medical Solutions USA recalled two units of its CT software applications on December 19, 2025. The software lacks FDA 510(k) clearance, posing potential risks to patients. Healthcare providers should stop using the affected software immediately.

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

MicroPort Recalls HIPTURN Fem Head Trial Device Over FDA Violation

Due to products not having FDA Premarket authorization to be distributed within the United States.

Tyber Medical Recalls VOLT Wrist Treatment System Over Thread Issue

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

Zydus Pharmaceuticals Recalls TraZODONE Tablets Over Defects

Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.