Z-1574-2026 Class II Ongoing
FDA device recall Z-1574-2026 was initiated by LeMaitre Vascular, Inc. on February 10, 2026 and is designated Class II. Reason for recall: Labeling mix-up resulting in the incorrect lot outer packaging of product. The recall status is ongoing. Affected quantity: 1 unit.
Recall Details
- Product Type
- Devices
- Report Date
- March 25, 2026
- Initiation Date
- February 10, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 unit
Product Description
Artegraft Vascular Graft; REF#: AG740;
Reason for Recall
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Distribution Pattern
US Nationwide distribution in the state of IL.
Code Information
REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;