cpsc regulated Recalls

Medline Electrophysiology Catheters Recalled Over Infection Risk

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 Industries Issues Recall of Catheters Over Infection Risk

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.

Medline ReNewal Catheters Recalled Due to Infection Risk

DPT Laboratories Recalls Diclofenac Sodium Gel Over PH Specification Failure

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.

Medline Industries Recalls Ultrasound Catheters Over Infection Risk

Baxter Healthcare Recalls Sterile Water for Irrigation Over Contamination

Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution

Philips North America Issues Recall for Patient Information Center Software

A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.

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

Tornier Recalls Surgical Screws Over Labeling Error

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

Canon Medical Recalls MRI Systems Over High-Pressure Hazard

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 Stent System Due to Deployment Issues

Gregory's Foods Cookie Dough Recalled for Undeclared Peanuts

Gregory's Foods recalled 308 cases of White Chocolate Macadamia Nut frozen cookie dough on December 19, 2025. The product contains undeclared peanuts, posing a serious allergy risk. Consumers should not consume the product and seek refunds.

Canon Medical MRI Systems Recalled Over High-Pressure Risk

Canon Medical Systems recalled 34 MRI systems due to a risk of helium gas release. The recall affects models MRT-3020 and MEXL-3020 distributed across 13 states. Healthcare providers should stop using these devices immediately and follow recall instructions.

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.

Tyber Medical Recalls VOLT Wrist Treatment System Due to Hazard

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