WhichRecall
Class IIReported 2026-03-25

Artegraft Vascular Graft; REF#: AG740;

Recalled by LeMaitre Vascular, Inc.

Reason for Recall

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

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Recall Number
Z-1574-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-02-10
Reported
2026-03-25
Distribution
US Nationwide distribution in the state of IL.
Code Info
REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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