SPINAL CORD STIMULATOR
This device is manufactured by BOSTON SCIENTIFIC - CORK, BOSTON SCIENTIFIC NEUROMODULATION, UNKNOWN.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Undesired Nerve Stimulation | 3 | Patient |
| 2024 | Thrombosis/Thrombus | 1 | Patient |
| 2024 | Swelling/ Edema | 2 | Patient |
| 2024 | Purulent Discharge | 1 | Patient |
| 2024 | Pain | 18 | Patient |
| 2024 | Numbness | 1 | Patient |
| 2024 | Neck Pain | 1 | Patient |
| 2024 | Nausea | 1 | Patient |
| 2024 | Muscle Weakness/Atrophy | 3 | Patient |
| 2024 | Ischemia Stroke | 1 | Patient |
| 2024 | Incontinence | 1 | Patient |
| 2024 | Implant Pain | 1 | Patient |
| 2024 | Hemorrhage/Blood Loss/Bleeding | 1 | Patient |
| 2024 | Headache | 1 | Patient |
| 2024 | Fluid Discharge | 1 | Patient |
| 2024 | Erythema | 1 | Patient |
| 2024 | Discomfort | 2 | Patient |
| 2024 | Cerebrospinal Fluid Leakage | 1 | Patient |
| 2024 | Bacterial Infection | 3 | Patient |
| 2024 | Apnea | 1 | Patient |
| 2024 | Aneurysm | 1 | Patient |
| 2024 | Abdominal Pain | 3 | Patient |
| 2024 | Wireless Communication Problem | 5 | Device |
| 2024 | Unexpected Therapeutic Results | 11 | Device |
| 2024 | Premature Discharge of Battery | 1 | Device |
| 2024 | Positioning Problem | 1 | Device |
| 2024 | Overheating of Device | 1 | Device |
| 2024 | Migration | 9 | Device |
| 2024 | High impedance | 10 | Device |
| 2024 | Fracture | 1 | Device |
| 2024 | Fire | 1 | Device |
| 2024 | Delayed Charge Time | 4 | Device |
| 2024 | Defective Device | 9 | Device |
| 2024 | Charging Problem | 22 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 32 | Device |
| 2023 | Vomiting | 1 | Patient |
| 2023 | Unspecified Infection | 1 | Patient |
| 2023 | Undesired Nerve Stimulation | 2 | Patient |
| 2023 | Twitching | 1 | Patient |
| 2023 | Swelling/ Edema | 1 | Patient |
| 2023 | Speech Disorder | 1 | Patient |
| 2023 | Purulent Discharge | 1 | Patient |
| 2023 | Paralysis | 1 | Patient |
| 2023 | Pain | 24 | Patient |
| 2023 | Numbness | 1 | Patient |
| 2023 | Muscle Weakness/Atrophy | 2 | Patient |
| 2023 | Inadequate Pain Relief | 2 | Patient |
| 2023 | Implant Pain | 2 | Patient |
| 2023 | Fluid Discharge | 2 | Patient |
| 2023 | Erosion | 1 | Patient |
| 2023 | Discomfort | 4 | Patient |
| 2023 | Diarrhea | 1 | Patient |
| 2023 | Device Overstimulation of Tissue | 1 | Patient |
| 2023 | Cramp(s) /Muscle Spasm(s) | 1 | Patient |
| 2023 | Convulsion/Seizure | 1 | Patient |
| 2023 | Chest Pain | 1 | Patient |
| 2023 | Bacterial Infection | 3 | Patient |
| 2023 | Wireless Communication Problem | 3 | Device |
| 2023 | Unexpected Therapeutic Results | 22 | Device |
| 2023 | Premature Discharge of Battery | 2 | Device |
| 2023 | Overheating of Device | 1 | Device |
| 2023 | Migration | 6 | Device |
| 2023 | Intermittent Energy Output | 1 | Device |
| 2023 | Inappropriate/Inadequate Shock/Stimulation | 1 | Device |
| 2023 | High impedance | 12 | Device |
| 2023 | Fracture | 3 | Device |
| 2023 | Device Displays Incorrect Message | 1 | Device |
| 2023 | Device Dislodged or Dislocated | 1 | Device |
| 2023 | Delayed Charge Time | 6 | Device |
| 2023 | Defective Device | 16 | Device |
| 2023 | Charging Problem | 42 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 21 | Device |
| 2022 | Undesired Nerve Stimulation | 2 | Patient |
| 2022 | Skin Inflammation/ Irritation | 2 | Patient |
| 2022 | Shock | 1 | Patient |
| 2022 | Pain | 9 | Patient |
| 2022 | Inadequate Pain Relief | 4 | Patient |
| 2022 | Implant Pain | 2 | Patient |
| 2022 | Fluid Discharge | 1 | Patient |
| 2022 | Erosion | 1 | Patient |
| 2022 | Discomfort | 2 | Patient |
| 2022 | Bacterial Infection | 1 | Patient |
| 2022 | Wireless Communication Problem | 1 | Device |
| 2022 | Use of Device Problem | 2 | Device |
| 2022 | Unexpected Therapeutic Results | 30 | Device |
| 2022 | Premature Discharge of Battery | 2 | Device |
| 2022 | Power Problem | 1 | Device |
| 2022 | Positioning Problem | 1 | Device |
| 2022 | Overheating of Device | 1 | Device |
| 2022 | Off-Label Use | 1 | Device |
| 2022 | Migration | 15 | Device |
| 2022 | Inappropriate/Inadequate Shock/Stimulation | 6 | Device |
| 2022 | High impedance | 12 | Device |
| 2022 | Fracture | 8 | Device |
| 2022 | Fire | 1 | Device |
| 2022 | Failure to Disconnect | 1 | Device |
| 2022 | Difficult to Insert | 1 | Device |
| 2022 | Device Dislodged or Dislocated | 3 | Device |
| 2022 | Delayed Charge Time | 2 | Device |
| 2022 | Defective Device | 21 | Device |
| 2022 | Charging Problem | 57 | Device |
| 2022 | Battery Problem | 1 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 23 | Device |
| 2021 | Insufficient Information | 1 | Patient |
| 2021 | Inadequate Pain Relief | 1 | Patient |
| 2021 | Unexpected Therapeutic Results | 6 | Device |
| 2021 | Migration | 2 | Device |
| 2021 | Inappropriate/Inadequate Shock/Stimulation | 1 | Device |
| 2021 | High impedance | 2 | Device |
| 2021 | Delayed Charge Time | 1 | Device |
| 2021 | Defective Device | 5 | Device |
| 2021 | Charging Problem | 23 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 5 | Device |
| 2020 | Pain | 1 | Patient |
| 2020 | Insufficient Information | 1 | Patient |
| 2020 | Inadequate Pain Relief | 1 | Patient |
| 2020 | Implant Pain | 1 | Patient |
| 2020 | Discomfort | 1 | Patient |
| 2020 | Wireless Communication Problem | 1 | Device |
| 2020 | Unexpected Therapeutic Results | 5 | Device |
| 2020 | Migration or Expulsion of Device | 1 | Device |
| 2020 | Migration | 1 | Device |
| 2020 | High impedance | 1 | Device |
| 2020 | Delayed Charge Time | 1 | Device |
| 2020 | Defective Device | 10 | Device |
| 2020 | Charging Problem | 11 | Device |
| 2020 | Adverse Event Without Identified Device or Use Problem | 3 | Device |