Recall Z-0103-2027— AVID Medical, Inc.

Class II · Ongoing

Class II FDA medical device recall by AVID Medical, Inc., initiated 2026-08-10. FDA's recall record names no specific 510(k) clearance for this event. Product: UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;. Reason: Product may be potentially contaminated with a lubricant used during the manufacturing process..

Recalling firm
AVID Medical, Inc.
Classification
Class II
Status
Ongoing
Initiated
2026-08-10
Firm location
Toano, VA, United States

Product description

UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;

Reason for recall

Product may be potentially contaminated with a lubricant used during the manufacturing process.

Data sourced from openFDA. This site is unofficial and independent of the FDA.