FDA recall Z-0072-2026

LeMaitre Vascular, Inc. · Class II · device

Product

Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is intended to serve as a substitute conduit for blood where bypass or replacement of occluded or diseased arterial segments is required or to establish a conduit for hemodialysis.

Reason for recall

Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.

Distribution

No US distribution. International distribution to Great Britian and Switzerland.

Key facts

Status
Ongoing
Initiation date
2025-08-25
Report date
2025-10-15
Voluntary/Mandated
Voluntary: Firm initiated
Location
North Brunswick, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0072-2026