Recall Z-1574-2026— LeMaitre Vascular, Inc.
Class II · Ongoing
Class II FDA medical device recall by LeMaitre Vascular, Inc., initiated 2026-02-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Artegraft Vascular Graft; REF#: AG740;. Reason: Labeling mix-up resulting in the incorrect lot outer packaging of product..
- Recalling firm
- LeMaitre Vascular, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-02-10
- Firm location
- North Brunswick, NJ, United States
Product description
Artegraft Vascular Graft; REF#: AG740;
Reason for recall
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Data sourced from openFDA. This site is unofficial and independent of the FDA.