Class I

Medical Device Recall: Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.

AVID Medical, Inc. · March 13, 2026

Reason for Recall

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.

Distribution

US distribution to FL, IL, MO, MS, NC, NE, TX.

States Affected

FL, IL, MO, MS, NC, NE, TX

Quantity Affected

6,956 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1972-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

AVID Medical, Inc. Medical Device Recall: Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05. | SafeCheck