United StatesLeMaitre Vascular Artegraft Collagen Vascular Graft, REF AG1015 (UDI‑DI 00316837000343, Lot/Serial 23MM581-016), distributed in Arkansas, is the product subject to this recall. The device was recalled because it was incorrectly packed in the wrong size labeled outer packaging and the recall is ongoing.
What's being recalled
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
Recalling firm: LeMaitre Vascular, Inc., North Brunswick, NJ, United States.
How to identify it
REF: AG1015; UDI-DI: 00316837000343; Lot/Serial Number: 23MM581-016;
The hazard
The device was incorrectly packed in the wrong size labeled outer packaging.
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 distribution to the state of: AR
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)