Avid Medical, Inc.: Cardiovascular Procedure Kit
Recall Summary AVID Medical is recalling the Halyard HEART CATH SELF REGIONAL kit (Model SELF131-05) because the syringe rotating adaptor may unwind during use, potentially causing the syringe to disconnect from the manifold. The kit was distributed to hospitals and medical facilities in Florida, Illinois, Missouri, Mississippi, North Carolina, Nebraska, and Texas.
- Recalling firm
- AVID Medical, Inc.
- Product
- Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
- 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 II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-13
- Status
- Open, Classified
- Areas affected
- FL, IL, MS, MO, NE, NC, TX
- Distribution
- US distribution to FL, IL, MO, MS, NC, NE, TX.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1d7561f4-f578-41dc-a1b3-4b2a0ad9b687