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High risk Medical DevicesClass I

AVID Medical Cardiac Cath Tray Shands JAX Recall

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

Updated March 13, 2026

AVID Medical has recalled the Halyard Cardiac Cath Tray Shands JAX kit (models SHND401-04 and SHND401-05) because a syringe rotating adapter inside the kit may unwind during use. This can cause a loose or complete disconnection between the syringe and manifold during a cardiac catheterization procedure, a serious risk to patient safety.

Is the AVID Medical, Inc. recalled? Yes. This product was recalled by FDA on March 13, 2026. Details below.

What is recalled

Halyard Cardiac Cath Tray Shands JAX kit, manufactured by AVID Medical, Inc. Affected model numbers: SHND401-04 and SHND401-05.

Am I affected

You are affected if your facility is using or has in stock the Halyard Cardiac Cath Tray Shands JAX kit with model number SHND401-04 or SHND401-05. Check the kit label or packaging for these model numbers.

What to do right now

Stop using any affected kits immediately. This recall was initiated by AVID Medical, Inc. No consumer contact information was provided in the recall record, contact AVID Medical directly or refer to the FDA recall notice at fda.gov/safety/recalls-market-withdrawals-safety-alerts for further instructions.

The 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.

Brands affected

AVID Medical, Inc.
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1972-2026
Classification
Class I
Recalled
March 13, 2026
Read the official notice

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