Device recall
Z-1283-2021: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot…
FDA device recall · Class II · In2Bones, SAS
Key facts
| Recall number (Z-number) | Z-1283-2021 |
|---|---|
| Recall event | 87341 |
| Product | In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery. |
| Product code | GFF |
| Recalling firm | In2Bones, SAS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2024 |
| FEI number | 3010470577 |
At a glance
- None 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