Recall Z-2409-2026— AVID Medical, Inc.

Name: FDA recall Z-2409-2026
Creator: U.S. Food and Drug Administration
Published: 2026-04-30

Class II · Ongoing

Class II FDA medical device recall by AVID Medical, Inc., initiated 2026-04-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard, Drape Pack. Kit Code: LMDP36-01.. Reason: Inadvertent distribution of sealed pouches that had not undergone validated sterilization..

Recalling firm: AVID Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2026-04-30
Firm location: Toano, VA, United States

Product description

Halyard, Drape Pack. Kit Code: LMDP36-01.

Reason for recall

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

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