Device recall
Z-2506-2021: CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product…
FDA device recall · Class II · In2bones USA, LLC
Key facts
| Recall number (Z-number) | Z-2506-2021 |
|---|---|
| Recall event | 88510 |
| Product | CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended for assisting surgeons in the manipulation of bone during surgical procedures. |
| Product code | LXH |
| Recalling firm | In2bones USA, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 8, 2023 |
| FEI number | 3011580264 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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