Lemaitre Vascular, Inc.: Tissue Graft Of 6mm And Greater
- Recalling firm
- LeMaitre Vascular, Inc.
- Product
- Artegraft Vascular Graft; REF#: AG740;
- Reason
- Labeling mix-up resulting in the incorrect lot outer packaging of product.
- Classification
- Class III
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-02-10
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of IL.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/f97661ac-0c85-41d8-b488-12fc4d637209