FDA recall Z-1574-2026
LeMaitre Vascular, Inc. · Class II · device
Product
Artegraft Vascular Graft; REF#: AG740;
Reason for recall
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Distribution
US Nationwide distribution in the state of IL.
Key facts
- Status
- Ongoing
- Initiation date
- 2026-02-10
- Report date
- 2026-03-25
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- North Brunswick, NJ, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1574-2026