Recall Z-2258-2025— AVID Medical, Inc.

Name: FDA recall Z-2258-2025
Creator: U.S. Food and Drug Administration
Published: 2025-06-11

Class II · Ongoing

Class II FDA medical device recall by AVID Medical, Inc., initiated 2025-06-11. FDA's recall record names no specific 510(k) clearance for this event. Product: MAJOR THORACOSCOPY BASIN. Medical convenience kit.. Reason: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration..

Recalling firm: AVID Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-06-11
Firm location: Toano, VA, United States

Product description

MAJOR THORACOSCOPY BASIN. Medical convenience kit.

Reason for recall

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

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