← FDA ENFORCEMENT
Z-1574-2026Class II

LeMaitre Vascular, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

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
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;

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. 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. Open the enforcement explorer →