Device recall
Z-1600-2016: Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model…
FDA device recall · Class II · Nuvectra
Key facts
| Recall number (Z-number) | Z-1600-2016 |
|---|---|
| Recall event | 73884 |
| Product | Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500. For use with Algovita Spinal Cord Stimulation Systems. The version of the software in the Clinician Programmer is v1.1.5. The Algovita Spinal Cord Stimulation system consists of a stimulator (EPG or IPG) that is… |
| Product code | LGW |
| Recalling firm | Nuvectra |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2017 |
| 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