AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE REF: KRIV26-02
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard IV START KIT NON-STERILE REF: KRIV26-02
- Reason
- Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Jul 14, 2026
- Reported
- Sep 23, 2026
- Distribution
- US Nationwide distribution in the state of NE.
- Status
- Ongoing
- Quantity
- 288 units
- Lot / codes
- Lot Number: 1658437 UDI: 10809160460481
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3108-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3108-2026 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.