AVID Medical, Inc. recalls Halyard ANTERIOR HIP PACK.
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.
- Reason
- A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Sep 8, 2026
- Reported
- Oct 28, 2026
- Distribution
- US Nationwide distributor in the state of Arizona.
- Status
- Ongoing
- Quantity
- 80 kits
- Lot / codes
- Model/Catalog Number: SOAH30. UDI-DI: 10809160520246. Lot Code: Lot Numbers: 1705826, 1705827. Expiration Date: 1/31/2028.
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0283-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0283-2027 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.