---
title: "Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M... — FDA record Z-0072-2026 | Is It on Recall"
description: "Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card."
url: https://isitonrecall.com/recall/fda-device-z-0072-2026-artegraft-collagen-vascular-graft-model-catalog-part-numbers-ag630m-ag636m-ag730m-ag740m-ag845m-the/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft ... — FDA record Z-0072-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 25, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is intended to serve as a substitute conduit for blood where bypass or replacement of occluded or diseased arterial segments is required or to establish a conduit for hemodialysis.
- **Reason**: Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
- **Classification**: Class II
- **Recalling firm**: LeMaitre Vascular, Inc.
- **Quantity**: 10 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0072-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0072-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model/Catalog/Part Number, UDI-DI (lot Numbers): 1. AG630M, 00316837000015 (24H361-021, 24H361-022, 24HH359-016). 2. AG636M, 00316837000022 (24H380-009). 3. AG730M, 00316837000060 (24H380-014, 24H380-004). 4. AG740M, 00316837000084 (24H380-003, 24H380-002). 5. AG845M, 00316837000138 (24HH350-017, 24HH359-011). Expiration date: 28 Jul 2027. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

No US distribution. International distribution to Great Britian and Switzerland.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 15, 2025
- **Recall initiation date**: Aug 25, 2025
- **Center classification date**: Oct 8, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0072-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [LeMaitre Vascular, Inc. records](https://isitonrecall.com/brand/lemaitre-vascular-inc/)