Device recall
Z-0922-2013: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is…
FDA device recall · Class II · Instratek, Incorporated
Key facts
| Recall number (Z-number) | Z-0922-2013 |
|---|---|
| Recall event | 63551 |
| Product | Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release procedures. |
| Product code | NBH |
| Recalling firm | Instratek, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 10, 2013 |
| FEI number | 1000118334 |
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