- Recalling firm
- AVID Medical, Inc.
- Reason for recall
- Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
- Affected products (lot / model / serial)
- Model/Catalog Number: LVEY27. UDI-DI: 10809160499528. Lot Numbers (Expiration Date): 1680076 (12/31/2026), 1680590 (6/30/2027).
- Units affected
- 260 kits
- Distribution pattern
- US Nationwide distribution in the state of California.
- Firm location
- Toano, VA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2763-2026
- Recall initiated
- May 7, 2026
- FDA classification date
- July 20, 2026
- FDA report date
- July 29, 2026
- FDA event ID
- 99249
- Last updated on HTM Vibe
- August 4, 2026