LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft; REF#: AG740;

Recall date

February 10, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1574-2026

FDA classification

Class II

Brand / firm

LeMaitre Vascular, Inc.

Sold / distributed

US Nationwide distribution in the state of IL.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Artegraft Vascular Graft; REF#: AG740;