immediate action Recalls

Beckman Coulter Sample Preparation System Recalled for Software Error

Medline Electrophysiology Catheters Recalled 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 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.

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

Medline Industries Recalls Ultrasound Catheters Over Infection Risk

Medline Catheters Recalled Over Infection Risk

DPT Laboratories Recalls Diclofenac Sodium Gel Over PH Specification Failure

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.

Medline ReNewal Catheters Recalled Due to Infection Risk

HANDELNINE GLOBAL Recalls Rheumacare Capsules Due to Lead Risk

CGMP Deviations: product found to contain lead.

Willy Pete's Chocolates Recalls Dark Chocolate Due to Almond Hazard

Almonds are not declared in the ingredient statement. Almond is included in description of product on front label.

Medline Industries Issues Recall of Catheters 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.

Atwater's Holiday Cookie Tin Recalled for Undeclared Tree Nuts

Atwater's recalled 197 Holiday Cookie Tins on December 21, 2025. The tins contain undeclared tree nut allergens including almonds, pecans, and walnuts. Consumers should not consume the product and seek refunds.

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

Tornier Recalls Surgical Screws Over Labeling Error

Tyber Medical Recalls VOLT Wrist Treatment System Over Thread Issue

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

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

Boston Scientific Recalls AXIOS Stent Due to Deployment Risks