COCHLEAR IMPLANT
This device is manufactured by ADVANCED BIONICS.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Vertigo | 1 | Patient |
| 2024 | Unspecified Infection | 1 | Patient |
| 2024 | Swelling/ Edema | 1 | Patient |
| 2024 | Pain | 1 | Patient |
| 2024 | Headache | 2 | Patient |
| 2024 | Head Injury | 2 | Patient |
| 2024 | Discomfort | 3 | Patient |
| 2024 | Bacterial Infection | 1 | Patient |
| 2024 | Appropriate Term / Code Not Available | 38 | Patient |
| 2024 | No Apparent Adverse Event | 1 | Device |
| 2024 | Migration | 1 | Device |
| 2024 | Mechanical Problem | 1 | Device |
| 2024 | Intermittent Communication Failure | 2 | Device |
| 2024 | Insufficient Information | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 34 | Device |
| 2023 | Undesired Nerve Stimulation | 1 | Patient |
| 2023 | Headache | 1 | Patient |
| 2023 | Appropriate Term / Code Not Available | 30 | Patient |
| 2023 | No Apparent Adverse Event | 2 | Device |
| 2023 | Misconnection | 1 | Device |
| 2023 | Loosening of Implant Not Related to Bone-Ingrowth | 2 | Device |
| 2023 | Loose or Intermittent Connection | 2 | Device |
| 2023 | Intermittent Communication Failure | 12 | Device |
| 2023 | Impedance Problem | 1 | Device |
| 2023 | Expulsion | 1 | Device |
| 2023 | Electrical /Electronic Property Problem | 2 | Device |
| 2023 | Circuit Failure | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 20 | Device |
| 2022 | Failure of Implant | 1 | Patient |
| 2022 | Appropriate Term / Code Not Available | 7 | Patient |
| 2022 | Patient Device Interaction Problem | 1 | Device |
| 2022 | Output below Specifications | 1 | Device |
| 2022 | Migration or Expulsion of Device | 1 | Device |
| 2022 | Migration | 2 | Device |
| 2022 | Mechanical Problem | 2 | Device |
| 2022 | Intermittent Communication Failure | 1 | Device |
| 2022 | Insufficient Information | 3 | Device |
| 2022 | Impedance Problem | 1 | Device |
| 2022 | Application Program Version or Upgrade Problem | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 13 | Device |
| 2021 | Insufficient Information | 1 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2020 | Appropriate Term / Code Not Available | 1 | Patient |
| 2020 | Output Problem | 1 | Device |
| 2020 | No Apparent Adverse Event | 1 | Device |
| 2020 | Loose or Intermittent Connection | 1 | Device |
| 2020 | Intermittent Communication Failure | 1 | Device |
| 2020 | Adverse Event Without Identified Device or Use Problem | 1 | Device |