FDA DeviceClass IINotable

FDA Recall: Artegraft Vascular Graft; REF#: AG740;

Date: 2026-03-25
Brand: LeMaitre Vascular, Inc.
Category: Medical Device
FDA Class: Class II

Description

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

Hazard

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

Remedy

1 unit

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