FDA Device recall Z-1574-2026
Artegraft Vascular Graft
- FDA Device
- Class II
- ongoing
- Published 2026-03-25
On 2026-03-25 the FDA classified a Class II recall of Artegraft Vascular Graft by Lemaitre Vascular, citing labeling mix-up resulting in the incorrect lot outer packaging of product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1574-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-10 |
| Published | 2026-03-25 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Lemaitre Vascular |
| Distribution | US |
Product
Artegraft Vascular Graft; REF#: AG740;
Reason
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Identifiers
| code_info | REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1574-2026%22
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