Class II

Medical Device Recall: Artegraft¿ Collagen Vascular Graft; REF: AG1015;

LeMaitre Vascular, Inc. · September 25, 2025

Reason for Recall

The device was incorrectly packed in the wrong size labeled outer packaging.

Distribution

US distribution to the state of: AR

States Affected

AR

Quantity Affected

1 unit

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0289-2026

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.

LeMaitre Vascular, Inc. Medical Device Recall: Artegraft¿ Collagen Vascular Graft; REF: AG1015; | SafeCheck