Class II

Medical Device Recall: Artegraft Vascular Graft; REF#: AG740;

LeMaitre Vascular, Inc. · February 10, 2026

Reason for Recall

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

Distribution

US Nationwide distribution in the state of IL.

States Affected

NATIONWIDE

Quantity Affected

1 unit

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1574-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.