Device recall
Z-0656-2010: Tornier Arthro Tunneler. For transossous fixation of tendons to bone in rotator…
FDA device recall · Class II · TAG Medical Corp.
Key facts
| Recall number (Z-number) | Z-0656-2010 |
|---|---|
| Recall event | 54036 |
| Product | Tornier Arthro Tunneler. For transossous fixation of tendons to bone in rotator cuff repair. Catalog Number: SMB000101 |
| Product code | NBH |
| Recalling firm | TAG Medical Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2016 |
| FEI number | 1000272060 |
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