AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK.
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
- Reason
- Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 19, 2026
- Reported
- Jul 29, 2026
- Distribution
- U.S. Nationwide distribution in the state of California.
- Status
- Ongoing
- Quantity
- 112 kits
- Lot / codes
- Model/Catalog Number: PVHM234-01. UDI-DI: 10809160416761. Lot Numbers (Expiration date): 1597314 (8/31/2026), 1599022 (5/31/2026).
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2772-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2772-2026 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.