FDA DeviceClass INotable
FDA Recall: Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Description
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.
Hazard
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.
Remedy
180 kits
Related Recalls
2026-05-13 · FDA_DEVICE
FDA Recall: Halyard CATH LAB kit. Model Number: SACL75-01.
AVID Medical, Inc.
2026-05-13 · FDA_DEVICE
FDA Recall: Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
AVID Medical, Inc.
2026-05-13 · FDA_DEVICE
FDA Recall: Halyard CATH LAB kit. Model Number: SACL75AM.
AVID Medical, Inc.
2026-05-13 · FDA_DEVICE
FDA Recall: Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
AVID Medical, Inc.