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Recall Observatory FDA recall evidence

Device product

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

Z-1972-2026

March 13, 2026

Class I

Product summary

Firm
AVID Medical, Inc.
Event
Event 98686
Status
Ongoing
Classification
Class I
Quantity
6,956 kits
Official record key
device-enforcement:Z-1972-2026

Official wording

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.

Code information: 1. Model Number: SHND401-04. UDI-DI (Kit Lot Numbers): 10809160395615 (1577749, 1577750, 1590780, 1590782, 1590783, 1590784, 1590785, 1590833, 1591141, 1591142, 1597561, 1600738, 1613343, 1622356, 1631890, 1643855, 1643856, 1643860, 1644853, 1645163, 1647458, 1647459, 1647460, 1650983, 1652365, 1652366). 2. Model Number: SHND401-05. UDI-DI (Kit Lot Numbers): 10809160491294 (1652367, 1668844, 1668845, 1668846, 1669188, 1669189, 1669504, 1669506, 1669507, 1671312, 1671313, 1671314, 1671315, 1671316).

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.