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Recall Observatory FDA recall evidence

Device 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.

Z-0072-2026

August 25, 2025

Class II

Product summary

Firm
LeMaitre Vascular, Inc.
Event
Event 97567
Status
Ongoing
Classification
Class II
Quantity
10 units
Official record key
device-enforcement:Z-0072-2026

Official wording

Reason: Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.

Code information: 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.

Distribution pattern: No US distribution. International distribution to Great Britian and Switzerland.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    label without CE and UKCA mark, missing