LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft
- Recalling company
- LeMaitre Vascular, Inc.
- Product
- Artegraft Vascular Graft; REF#: AG740;
- Reason
- Labeling mix-up resulting in the incorrect lot outer packaging of product.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 10, 2026
- Reported
- Mar 25, 2026
- Distribution
- US Nationwide distribution in the state of IL.
- Status
- Ongoing
- Quantity
- 1 unit
- Lot / codes
- REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
- Company location
- North Brunswick, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1574-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1574-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.