SCS EXTENSION
This device is manufactured by ABBOTT MEDICAL, ADVANCED NEUROMODULATION SYSTEMS, ST JUDE MED - NEUROMODULATION, ST JUDE MEDICAL, ST JUDE MEDICAL - NEUROMODULATION and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Undesired Nerve Stimulation | 1 | Patient |
| 2024 | Post Operative Wound Infection | 2 | Patient |
| 2024 | Inadequate Pain Relief | 5 | Patient |
| 2024 | Implant Pain | 2 | Patient |
| 2024 | Failure of Implant | 3 | Patient |
| 2024 | Impedance Problem | 2 | Device |
| 2024 | High impedance | 3 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2023 | Unspecified Infection | 2 | Patient |
| 2023 | Undesired Nerve Stimulation | 1 | Patient |
| 2023 | Nausea | 1 | Patient |
| 2023 | Inadequate Pain Relief | 9 | Patient |
| 2023 | Headache | 1 | Patient |
| 2023 | Material Twisted/Bent | 2 | Device |
| 2023 | Impedance Problem | 1 | Device |
| 2023 | High impedance | 3 | Device |
| 2023 | Fracture | 2 | Device |
| 2023 | Disconnection | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2022 | Use of Device Problem | 2 | Device |
| 2022 | High impedance | 4 | Device |
| 2022 | Fracture | 3 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 2 | Device |