Recall Z-1002-2026— AVID Medical, Inc.

Name: FDA recall Z-1002-2026
Creator: U.S. Food and Drug Administration
Published: 2025-11-11

Class I · Ongoing

Class I FDA medical device recall by AVID Medical, Inc., initiated 2025-11-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08. Reason: Devices are not suitable for organ transplant..

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

Product description

Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

Reason for recall

Devices are not suitable for organ transplant.

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