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FDAFebruary 10, 2026device

Artegraft Vascular Graft; REF#: AG740;

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

lemaitre vascularlemaitre

UPCs

00316837000299

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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