STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
This device is manufactured by MEDTRONIC MED REL MEDTRONIC PUERTO RICO, MEDTRONIC PUERTO RICO OPERATIONS CO.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Undesired Nerve Stimulation | 1 | Patient |
2024 | Bruise/Contusion | 1 | Patient |
2024 | Therapy Delivered to Incorrect Body Area | 1 | Device |
2024 | Migration or Expulsion of Device | 1 | Device |
2024 | Insufficient Information | 1 | Device |
2024 | Battery Problem | 1 | Device |
2023 | Unspecified Tissue Injury | 1 | Patient |
2023 | Undesired Nerve Stimulation | 1 | Patient |
2023 | Pain | 1 | Patient |
2023 | Insufficient Information | 1 | Patient |
2023 | Electric Shock | 1 | Patient |
2023 | Discomfort | 1 | Patient |
2023 | Device Embedded In Tissue or Plaque | 1 | Patient |
2023 | Therapy Delivered to Incorrect Body Area | 1 | Device |
2023 | Patient Device Interaction Problem | 1 | Device |
2023 | Insufficient Information | 1 | Device |
2023 | Inappropriate/Inadequate Shock/Stimulation | 1 | Device |
2023 | Energy Output Problem | 1 | Device |
2023 | Battery Problem | 1 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2021 | Insufficient Information | 1 | Device |
2021 | Device Operates Differently Than Expected | 1 | Device |
2021 | Charging Problem | 1 | Device |
2021 | Battery Problem | 1 | Device |
2020 | Unintended Collision | 1 | Device |
2020 | Insufficient Information | 1 | Device |
2020 | Device Operates Differently Than Expected | 1 | Device |
2020 | Battery Problem | 1 | Device |