Artegraft Vascular Graft recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIOngoing
Summary: LeMaitre Vascular, Inc. is recalling Artegraft Vascular Graft; REF#: AG740;. Reason: Labeling mix-up resulting in the incorrect lot outer packaging of product.
What is being recalled
Artegraft Vascular Graft; REF#: AG740;
Why
Labeling mix-up resulting in the incorrect lot outer packaging of product.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the state of IL. (states named: Illinois)
How to tell if yours is affected
REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1574-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | February 10, 2026 |
| Reported | March 25, 2026 |
| Company | LeMaitre Vascular, Inc. |
| Company location | North Brunswick, NJ, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1 unit |
More recalls from LeMaitre Vascular, Inc. · all medical device recalls · recalls from February 2026