DIXI MEDICAL USA
DIXI MEDICAL USA appears in FDA public data with 9 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0535-2022, Class II) was initiated on December 9, 2021.
Summary
- Total Recalls
- 9
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0535-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0541-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0540-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0538-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0542-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0537-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0536-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0534-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |
| Z-0539-2022 | Class II | The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth | December 9, 2021 |