Avid Medical, Inc.: Cardiac Catheterization Kit

Recalling firm
AVID Medical, Inc.
Product
Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
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/46f139ec-8e8f-487e-82fd-514c14b15591