Recall Z-2763-2026— AVID Medical, Inc.
Class II · Ongoing
Class II FDA medical device recall by AVID Medical, Inc., initiated 2026-05-07. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.. Reason: Incorrect concentration of Betadine solution contained within certain AVID convenience kits..
- Recalling firm
- AVID Medical, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-05-07
- Firm location
- Toano, VA, United States
Product description
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Reason for recall
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Data sourced from openFDA. This site is unofficial and independent of the FDA.