Nuvectra recalls
Nuvectra appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2016-12-28.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 2 |
|---|---|
| Published | 2016-05-11 to 2016-12-28 |
| By agency | FDA Device (2) |
| By classification | Class II (2) |
| By status | terminated (2) |
| Distribution named in notices | US |
Recalls
- Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit
FDA Device · Class II · 2016-12-28 · Nuvectra
Reason: Nuvectra is conducting a recall due to two clinical risks that are associated with certain percutaneous leads currently being used in the Algovita Spinal Cord Stimulation System. It has been reported that in some percut… - Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500
FDA Device · Class II · 2016-05-11 · Nuvectra
Reason: If used, the optional Swap feature copies programming parameters from the external pulse generator (EPG) as well as unintended calibration data to the implantable pulse generator (lPG). This may result in the user being…