Device recall
Z-0072-2026: Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M…
FDA device recall · Class II · LeMaitre Vascular, Inc.
Key facts
| Recall number (Z-number) | Z-0072-2026 |
|---|---|
| Recall event | 97567 |
| Product | Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is intended to serve as a substitute conduit for blood where bypass or replacement of occluded or diseased arterial segments is required or to establish a conduit for hemodialysis. |
| Product code | LXA |
| Recalling firm | LeMaitre Vascular, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000121696 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database