Recall Z-1741-2025— AVID Medical, Inc.

Name: FDA recall Z-1741-2025
Creator: U.S. Food and Drug Administration
Published: 2025-03-31

Class II · Ongoing

Class II FDA medical device recall by AVID Medical, Inc., initiated 2025-03-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit. Reason: An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use..

Recalling firm: AVID Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-03-31
Firm location: Toano, VA, United States

Product description

Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit

Reason for recall

An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.

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