QiG Group LLC
QiG Group LLC appears in FDA public data with 3 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1192-2016, Class II) was initiated on January 26, 2016.
Summary
- Total Recalls
- 3
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1192-2016 | Class II | Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel) | January 26, 2016 |
| Z-1193-2016 | Class II | Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel) | January 26, 2016 |
| Z-1194-2016 | Class II | Algostim LLC, Algovita External Pulse Generator, Trial Stimulator, Model 3400 | January 26, 2016 |