Artegraft Vascular Graft — Class II medical device recall Z-1574-2026
Ongoing recall by LeMaitre Vascular, Inc., reported 2026-03-25, distributed nationwide. Labeling mix-up resulting in the incorrect lot outer packaging of product.
| Recall number | Z-1574-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | LeMaitre Vascular, Inc., North Brunswick, NJ, United States |
| Recall initiated | 2026-02-10 |
| Classified | 2026-03-19 |
| Reported by FDA | 2026-03-25 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00316837000299 |
| Serial numbers | 24GG298-022 |
| Model numbers | AG740 |
| Expiration dates | 2027-06-28 |
Product
Artegraft Vascular Graft; REF#: AG740;
Reason for recall
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1574-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.