Device recall
Z-0834-2025: Cook Medical Biodesign Dural Graft, REF C-DUR-7X10, REF G31091, Sterile
FDA device recall · Class II · Cook Biotech, Inc.
Key facts
| Recall number (Z-number) | Z-0834-2025 |
|---|---|
| Recall event | 95961 |
| Product | Cook Medical Biodesign Dural Graft, REF C-DUR-7X10, REF G31091, Sterile |
| Product code | GXQ |
| Recalling firm | Cook Biotech, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K160869 |
| FEI number | 3002340648 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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