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LeMaitre Vascular, Inc. recalls Artegraft¿ Collagen Vascular Graft; REF: AG1015;
Recalled October 29, 2025 · FDA recall Z-0289-2026 · LeMaitre Vascular
Hazard
The device was incorrectly packed in the wrong size labeled outer packaging. · FDA Class II
Units
1 unit
Sold at
US distribution to the state of: AR
Description
The device was incorrectly packed in the wrong size labeled outer packaging.
Product
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
Manufacturer(s)
LeMaitre Vascular, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →