SCS IPG
This device is manufactured by ABBOTT MEDICAL, ADVANCED NEUROMODULATION SYSTEMS, SJM NEUROMODULATION DIVISION, ST JUDE - NEUROMODULATION, ST JUDE MED - NEUROMODULATION and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Insufficient Information | 11 | Patient |
| 2024 | Inadequate Pain Relief | 33 | Patient |
| 2024 | Implant Pain | 4 | Patient |
| 2024 | Failure of Implant | 1 | Patient |
| 2024 | Burning Sensation | 2 | Patient |
| 2024 | Wireless Communication Problem | 15 | Device |
| 2024 | Temperature Problem | 1 | Device |
| 2024 | Premature Discharge of Battery | 3 | Device |
| 2024 | No Apparent Adverse Event | 2 | Device |
| 2024 | Migration | 1 | Device |
| 2024 | Insufficient Information | 8 | Device |
| 2024 | Improper or Incorrect Procedure or Method | 11 | Device |
| 2024 | High impedance | 1 | Device |
| 2024 | Delayed Charge Time | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2023 | Unspecified Infection | 1 | Patient |
| 2023 | Insufficient Information | 12 | Patient |
| 2023 | Inadequate Pain Relief | 50 | Patient |
| 2023 | Implant Pain | 5 | Patient |
| 2023 | Failure of Implant | 5 | Patient |
| 2023 | Wireless Communication Problem | 33 | Device |
| 2023 | Use of Device Problem | 1 | Device |
| 2023 | No Device Output | 1 | Device |
| 2023 | Migration | 1 | Device |
| 2023 | Insufficient Information | 9 | Device |
| 2023 | Improper or Incorrect Procedure or Method | 16 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 5 | Device |
| 2022 | Inadequate Pain Relief | 22 | Patient |
| 2022 | Failure of Implant | 2 | Patient |
| 2022 | Wireless Communication Problem | 64 | Device |
| 2022 | Use of Device Problem | 4 | Device |
| 2022 | Temperature Problem | 1 | Device |
| 2022 | Premature Discharge of Battery | 5 | Device |
| 2022 | Nonstandard Device | 1 | Device |
| 2022 | No Device Output | 1 | Device |
| 2022 | Insufficient Information | 6 | Device |
| 2022 | Improper or Incorrect Procedure or Method | 41 | Device |
| 2022 | Battery Problem | 3 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2021 | Inadequate Pain Relief | 6 | Patient |
| 2021 | Implant Pain | 1 | Patient |
| 2021 | Failure of Implant | 1 | Patient |
| 2021 | Wireless Communication Problem | 3 | Device |
| 2021 | Use of Device Problem | 5 | Device |
| 2021 | Migration | 1 | Device |
| 2021 | Improper or Incorrect Procedure or Method | 11 | Device |
| 2020 | Insufficient Information | 1 | Patient |
| 2020 | Inadequate Pain Relief | 7 | Patient |
| 2020 | Failure of Implant | 1 | Patient |
| 2020 | Wireless Communication Problem | 4 | Device |
| 2020 | Use of Device Problem | 3 | Device |
| 2020 | Premature Discharge of Battery | 1 | Device |
| 2020 | Improper or Incorrect Procedure or Method | 9 | Device |
| 2020 | Device Inoperable | 1 | Device |
| 2020 | Charging Problem | 1 | Device |
| 2020 | Adverse Event Without Identified Device or Use Problem | 5 | Device |