LeMaitre Vascular, Inc. recalls

7 recalls on record · latest: February 10, 2026

Official U.S. recall history for LeMaitre Vascular, Inc., compiled from official government records.

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LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft; REF#: AG740;

February 10, 2026 · Medical device recalls Moderate risk Labeling mix-up resulting in the incorrect lot outer packaging of product.

LeMaitre Vascular, Inc. recalls Artegraft¿ Collagen Vascular Graft; REF: AG1015;

September 25, 2025 · Medical device recalls Moderate risk The device was incorrectly packed in the wrong size labeled outer packaging.

LeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630, (3) AG 636, (4) AG 640, (5) AG 645, (6) AG 71…

September 2, 2025 · Medical device recalls Moderate risk The bovine carotid arteries used to produce the impacted grafts from affected l…

Artegraft Collagen Vascular Graft recalled over labeling errors

August 25, 2025 · Medical device recalls Moderate risk Devices were distributed with incorrect label without CE and UKCA mark, missing…

LeMaitre Vascular, Inc. recalls Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.

April 11, 2025 · Medical device recalls Moderate risk During internal product testing, it was observed that some packages to have inc…

LeMaitre Vascular, Inc. recalls TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1…

April 11, 2025 · Medical device recalls Moderate risk During internal product testing, it was observed that some packages to have inc…

LeMaitre Vascular, Inc. recalls Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56

April 11, 2025 · Medical device recalls Moderate risk During internal product testing, it was observed that some packages to have inc…