Z-3261-2026 Class II Ongoing
FDA device recall Z-3261-2026 was initiated by AVID Medical, Inc. on Jul 22, 2026 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 192 kits (4 cases).
Recall Details
- Product Type
- Devices
- Report Date
- Sep 30, 2026
- Initiation Date
- Jul 22, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 192 kits (4 cases)
Product Description
Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-01
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.
Distribution Pattern
US Nationwide distribution.
Code Information
Kit Model Number: KRIV26-01. UDI-DI: 10809160450109. Lot Number: 1642214. Expiration Date: 7/31/2027