AVID Medical, Inc. recalls Halyard MINI PLUS KIT SOUTH
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
- Reason
- Devices are not suitable for organ transplant.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Nov 11, 2025
- Reported
- Jan 14, 2026
- Distribution
- US Nationwide distribution in the states of FL, GA and Puerto Rico.
- Status
- Ongoing
- Quantity
- 380 units
- Lot / codes
- Kit Code: JACK097-08; UDI : 10809160462829; Lot No: 1654185.
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1002-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1002-2026 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.