← FDA ENFORCEMENT
Z-1574-2026Class II

LeMaitre Vascular, Inc.

Recalling firm
LeMaitre Vascular, Inc.
Product type
Device
Status
Ongoing
Report date
2026-03-25
Distribution
US Nationwide distribution in the state of IL.
Firm state
NJ
Product quantity
1 unit
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

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

Product description

Artegraft Vascular Graft; REF#: AG740;

Code / lot info

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

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.