Artegraft Vascular Graft recall: Labeling Error
Artegraft Vascular Graft; REF#: AG740;
Why was Artegraft Vascular Graft recalled?
Labeling mix-up resulting in the incorrect lot outer packaging of product.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
- Product
- Artegraft Vascular Graft; REF#: AG740;
- Recalling firm
- LeMaitre Vascular, Inc.
- Quantity
- 1 unit
- Distribution
- US Nationwide distribution in the state of IL.
- Recall date
- March 25, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)