Artegraft Vascular Graft recallZ-1574-2026 · LeMaitre Vascular, Inc. · initiated Feb 10, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from LeMaitre Vascular, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Labeling mix-up resulting in the incorrect lot outer packaging of product.
FDA root cause category: Labeling Change Control
What the company is doing
On February 10, 2026 URGENT: MEDICAL DEVICE RECALL letters were sent to customers. Actions to be taken: 1. Check your inventory against the list of lots in this letter. Immediately quarantine any recalled devices. 2. Complete the form at the end of this letter. Please note that you must return the form even if you have no devices in inventory. 3. If the product has been implanted, graft explantation/patient intervention is NOT required. 4. Scan the reply form and send it to [email protected]. 5. When a recalled device has been returned to LeMaitre Vascular, a replacement device will be provided. 6. If you have transferred devices to another facility, please forward a copy of this recall letter to them. If you have any questions, contact Monte Nelson; [email protected]; 732-422-8333 Monday through Friday, 8:00 AM to 4:30 PM, Eastern Time, or email [email protected]
Recall details
- Recall number
- Z-1574-2026
- Status
- Open, Classified
- Initiated by the company
- Feb 10, 2026
- Posted by the FDA
- Mar 19, 2026
- Recalling firm
- LeMaitre Vascular, Inc.
- Quantity
- 1 unit
- Product code
- LXA
- Distribution
- US Nationwide distribution in the state of IL.
Product description
Artegraft Vascular Graft; REF#: AG740;
Code information (models, lots, serial numbers)
REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Artegraft Vascular Graft AG 740Lemaitre Vascular, Inc. · Tissue Graft Of 6mm And Greater2 recalls5 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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