Class I U.S. Food and Drug Administration

AVID Medical, Inc. Halyard Organ Recovery OR Pack, Kit Code: Llof1000-17 recall: Devices are not suitable for organ transplant

Recall published 9 months ago

Devices are not suitable for organ transplant.

The hazard: Device safety concern

A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.

What the notice says: Devices are not suitable for organ transplant.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-1001-2026
Published
January 14, 2026
Risk level
Class I
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
AVID Medical, Inc.
Product type
Medical devices
Units affected
52 units
Distribution
Nationwide
Made in
United States
Lot / code info
Kit Code: LLOF1000-17; UDI : 10809160460726, Lot No : 1651709
UPC codes
10809160460726

Products covered by this recall

Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

Check your product

The notice names 2 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 10809160460726

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 1651709 — 52 units

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

AVID Medical, Inc. — A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If you are a facility, quarantine affected stock and log the correction.
  3. Report device problems to the FDA through MedWatch.
  4. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.

Claiming on a recalled device

Device recalls are tracked by serial and lot number, so your claim moves faster if you lead with those.

  • Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.
  • Ask explicitly whether your unit is in the affected range; many recalls cover only part of a model line.
  • If you need the device daily, ask what interim arrangement they offer while the remedy is carried out.
  • Log the date, the name and the reference number of every call. Device recalls can run for months.

Company contact: AVID Medical, Inc. — 9000 Westmont Dr, Toano, VA, 23168-9351

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was AVID Medical, Inc. medical devices recalled?

Devices are not suitable for organ transplant. Devices are not suitable for organ transplant.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 10809160460726; lot code 1651709 — 52 units. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.

Where was the recalled product sold?

It was distributed nationwide.

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