Device recall
Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02
- Recall number
- Z-3260-2026
- Event id
- 99764
- Status
- Ongoing
- FDA classification
- Class II
- Recalling firm
- AVID Medical, Inc.
- Report date
- Sep 30, 2026
- Posted
- Sep 23, 2026
- Initiated
- Jul 22, 2026
- Center classification date
- Sep 23, 2026
- Product code
- LRO
- Device type
- General Surgery Tray
- Reason
- Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
- Root cause
- Packaging process control
- Quantity
- 816 kits (17 cases)
- Code info
- 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).
- Distribution
- US Nationwide distribution.
- Voluntary or mandated
- Voluntary: Firm initiated
- Location
- Toano, VA, United States