Device recall
Z-0469-2016: Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with…
FDA device recall · Class II · Instratek, Incorporated
Key facts
| Recall number (Z-number) | Z-0469-2016 |
|---|---|
| Recall event | 72748 |
| Product | Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression (ETTD) System. |
| Product code | HRX |
| Recalling firm | Instratek, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2016 |
| FEI number | 1000118334 |
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