FDAFDA recall Z-3260-2026 · Sep 30, 2026
AVID Medical, Inc.: Halyard IV START KIT NON-STERILE recall
Recall found
Product
Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- 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).
- Quantity
- 816 kits (17 cases)
- Distribution
- US Nationwide distribution.
- Recalling firm
- AVID Medical, Inc., Toano, VA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-22
Source: openFDA enforcement record Z-3260-2026 · search recall number Z-3260-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.