Recall Z-0283-2027— AVID Medical, Inc.

Name: FDA recall Z-0283-2027
Creator: U.S. Food and Drug Administration
Published: 2026-09-08

Class II · Ongoing

Class II FDA medical device recall by AVID Medical, Inc., initiated 2026-09-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.. Reason: A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications..

Recalling firm: AVID Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2026-09-08
Firm location: Toano, VA, United States

Product description

Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.

Reason for recall

A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.

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