AVID Medical, Inc. 2026-05-13 Health critical FDA
Health · FDA · Recall #FDA-Z-1972-2026
Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05. Recall
Issued May 13, 2026 · AVID Medical, Inc.
In May 2026, AVID Medical, Inc. recalled the Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05., a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact AVID Medical, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- AVID Medical, Inc.
- Category
- Health
- Recall date
- May 13, 2026
- Units affected
- Not reported
- Sold at
- US distribution to FL, IL, MO, MS, NC, NE, TX.
- Recall number
- FDA-Z-1972-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- AVID Medical, Inc. has 9 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.