AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02
- Reason
- Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 22, 2026
- Reported
- Sep 30, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 816 kits (17 cases)
- Lot / codes
- 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).
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3260-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3260-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.