LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft

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

Artegraft Vascular Graft; REF#: AG740;

On February 10, 2026 URGENT: MEDICAL DEVICE RECALL letters were sent to customers. Actions to be taken: 1. Check your inventory against the list of lots in this letter. Immediately quarantine any recalled devices. 2. Complete the form at the end of this letter. Please note that you must return the form even if you have no devices in inventory. 3. If the product has been implanted, graft explantation/patient intervention is NOT required. 4. Scan the reply form and send it to recalls@lemaitre.com. 5. When a recalled device has been returned to LeMaitre Vascular, a replacement device will be provided. 6. If you have transferred devices to another facility, please forward a copy of this recall letter to them. If you have any questions, contact Monte Nelson; mnelson@lemaitre.com; 732-422-8333 Monday through Friday, 8:00 AM to 4:30 PM, Eastern Time, or email Recalls@lemaitre.com

• FDA enforcement recordOfficial FDA database entry for Z-1574-2026
• FDA device classification · LXAOfficial FDA classification for this device type
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find LeMaitre Vascular, Inc.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.