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Recall Observatory FDA recall evidence

Device product

Artegraft Vascular Graft; REF#: AG740;

Z-1574-2026

February 10, 2026

Class II

Product summary

Firm
LeMaitre Vascular, Inc.
Event
Event 98409
Status
Ongoing
Classification
Class II
Quantity
1 unit
Official record key
device-enforcement:Z-1574-2026

Official wording

Reason: Labeling mix-up resulting in the incorrect lot outer packaging of product.

Code information: REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;

Distribution pattern: US Nationwide distribution in the state of IL.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Labeling mix-up resulting in the incorrect