AVID Medical Halyard MINI PLUS Kit South: Not Suitable for Organ Transplant

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Contact the company & request your remedy

Recalling firmAVID Medical, Inc.9000 Westmont Dr · Toano, VA 23168-9351

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

AVID Medical is recalling the Haly:ry MINI PLUS Kit South (Kit Code JACK097-08) because it is not designed for organ transplant use. This could pose a serious risk if used incorrectly in such procedures.

Why it’s dangerous

The kit is not designed for organ transplant procedures, which could lead to serious complications if used incorrectly. This is a critical safety issue for medical applications.

Who’s affected

Healthcare professionals and organ transplant facilities that use this kit for procedures. Those handling the kit without proper medical training are at highest risk.

How to tell if you have this one

Check for Kit Code JACK097-08 on the product. Units also have UDI: 10809160462829 and Lot No: 1654185. This kit is sold for organ transplant procedures.

Brand
AVID Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Now
Immediately stop using the Halyard MINI PLUS Kit South (Kit Code JACK097-08) as it is not suitable for organ transplant procedures.

✎ GovInfoNow

Questions people ask

Is this kit safe for organ transplants?

No, this kit is not designed for organ transplant procedures and should not be used for that purpose.

How can I identify the recalled kit?

Look for Kit Code JACK097-08, UDI: 10809160462829, and Lot No: 1654185 on the product.

What should I do if I have this kit?

Immediately stop using it and contact AVID Medical for further instructions.

Take action

Contact AVID Medical

We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1002-2026 — AVID Medical AVID Medical

Hello,

I own a AVID Medical that is covered by recall Z-1002-2026 from AVID Medical.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1002-2026 (November 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1002-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

AVID Medical, Inc. recalls Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

Stop using this now