AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit.
- Recalling company
- AVID Medical, Inc.
- Product
- Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
- Reason
- Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Mar 13, 2026
- Reported
- May 13, 2026
- Distribution
- US distribution to FL, IL, MO, MS, NC, NE, TX.
- Status
- Ongoing
- Quantity
- 222 kits
- Lot / codes
- 1. Model Number: EAMC1000-05. UDI-DI (Kit Lot Numbers): 10809160377314 (1573593, 1583827, 1609541, 1609725, 1612134, 1612516, 1619132, 1623384, 1627013, 1635459, 1672306, 1675159). 2. Model Number: WAFB208-02. UDI-DI (Kit Lot Numbers): 10809160424759 (1615954, 1653009).
- Company location
- Toano, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1970-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1970-2026 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.