Device recall
Z-1192-2016: Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8…
FDA device recall · Class II · QiG Group LLC
Key facts
| Recall number (Z-number) | Z-1192-2016 |
|---|---|
| Recall event | 73150 |
| Product | Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel) |
| Product code | LGW |
| Recalling firm | QiG Group LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2017 |
| PMA numbers | P130028 |
| FEI number | 3010109865 |
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