LeMaitre Vascular, Inc.: Artegraft Vascular Graft; REF#: AG740;
Read the official notice at FDA (device) →
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- LeMaitre Vascular, Inc.
- Product
- Artegraft Vascular Graft; REF#: AG740;
- Reason / hazard
- Labeling mix-up resulting in the incorrect lot outer packaging of product.
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- US Nationwide distribution in the state of IL.
- Recall initiated
- 2026-02-10
- Code info
- REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
- Product quantity
- 1 unit
- Voluntary mandated
- Voluntary: Firm initiated
- City
- North Brunswick
- State
- NJ
- Country
- United States
- Event id
- 98409
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