FDA DevicesClass II
Artegraft Vascular Graft; REF#: AG740;
Published: March 25, 2026Recall ID: Z-1574-2026Category: devicesCountry: US
Reason for Recall / Hazard
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Product Description & Identification
Artegraft Vascular Graft; REF#: AG740;
Affected Products
Artegraft Vascular Graft; REF#: AG740;
Additional Source Details
| Field | Value |
|---|---|
| City | North Brunswick |
| State | NJ |
| Event id | 98409 |
| Address 1 | 206 N Center Dr |
| Address 2 | N/A |
| Code info | REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027; |
| Postal code | 08902-4246 |
| Report date | 20260325 |
| Product type | Devices |
| Product quantity | 1 unit |
| Reason for recall | Labeling mix-up resulting in the incorrect lot outer packaging of product. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260210 |
| Initial firm notification | Letter |
| Center classification date | 20260319 |
Overview
- Recalling FirmLeMaitre Vascular, Inc.
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the state of IL.