LeMaitre Vascular, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0289-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Artegraft¿ Collagen Vascular Graft; REF: AG1015;

Product Classification:

Class II

Date Initiated: September 25, 2025

Date Posted: October 29, 2025

Recall Number: Z-0289-2026

Event ID: 97700

Reason for Recall:

The device was incorrectly packed in the wrong size labeled outer packaging.

Status: Ongoing

Product Quantity: 1 unit

Code Information:

REF: AG1015; UDI-DI: 00316837000343; Lot/Serial Number: 23MM581-016;

Distribution Pattern:

US distribution to the state of: AR

Voluntary or Mandated:

Voluntary: Firm initiated