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LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft; REF#: AG740;
Recalled March 25, 2026 · FDA recall Z-1574-2026 · LeMaitre Vascular
Hazard
Labeling mix-up resulting in the incorrect lot outer packaging of product. · FDA Class II
Units
1 unit
Sold at
US Nationwide distribution in the state of IL.
Description
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Product
Artegraft Vascular Graft; REF#: AG740;
Manufacturer(s)
LeMaitre Vascular, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →