United StatesLeMaitre Vascular Artegraft Vascular Graft, REF#: AG740 (UDI‑DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027) is being recalled. The recall was initiated because of a labeling mix-up resulting in incorrect lot outer packaging; the unit was distributed in Illinois.
What's being recalled
Artegraft Vascular Graft; REF#: AG740;
Recalling firm: LeMaitre Vascular, Inc., North Brunswick, NJ, United States.
How to identify it
REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
The hazard
Labeling mix-up resulting in the incorrect lot outer packaging of product.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the state of IL.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)