Device recall
Z-0781-2017: Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode…
FDA device recall · Class II · Nuvectra
Key facts
| Recall number (Z-number) | Z-0781-2017 |
|---|---|
| Recall event | 75459 |
| Product | Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Leads, 12-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Trial Leads, 8-electrode Lead Kit; Algovita Spinal Cord… |
| Product code | LGW |
| Recalling firm | Nuvectra |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 8, 2018 |
| PMA numbers | P130028 |
| FEI number | 3010309840 |
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