- Recalling firm
- AVID Medical, Inc.
- Reason for recall
- Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
- Affected products (lot / model / serial)
- Kit Model Number: KRIV26-02. UDI-DI: 10809160460481. Lot Numbers (Expiration Date): 1658438 (07/31/2026), 1685838 (12/19/2027), 1699753 (02/28/2027), 1706455 (12/19/2027).
- Units affected
- 816 kits (17 cases)
- Distribution pattern
- US Nationwide distribution.
- 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-3260-2026
- Recall initiated
- July 22, 2026
- FDA classification date
- September 23, 2026
- FDA report date
- September 30, 2026
- FDA event ID
- 99764
- Last updated on HTM Vibe
- October 6, 2026
