Official recall notice
FDA DeviceClass IINotable
FDA Recall: Artegraft Vascular Graft; REF#: AG740;
- Recall date
- 2026-03-25
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Labeling mix-up resulting in the incorrect lot outer packaging of product.
Recommended action
What to do
1 unit
Product description
Labeling mix-up resulting in the incorrect lot outer packaging of product.