Recall Z-1338-2026— AVID Medical, Inc.

Name: FDA recall Z-1338-2026
Creator: U.S. Food and Drug Administration
Published: 2026-01-02

Class II · Ongoing

Class II FDA medical device recall by AVID Medical, Inc., initiated 2026-01-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.. Reason: Tyvek bag seal issue which may compromise sterility of the kit..

Recalling firm: AVID Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2026-01-02
Firm location: Toano, VA, United States

Product description

Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.

Reason for recall

Tyvek bag seal issue which may compromise sterility of the kit.

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