IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
This device is manufactured by 3M HEALTH CARE, BOSTON SCIENTIFIC, BOSTON SCIENTIFIC CORPORATION, CAMERON HEALTH, GENERIC MEDICAL DEVICES and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Shock from Patient Lead(s) | 2 | Patient |
| 2024 | Electric Shock | 1 | Patient |
| 2024 | Bacterial Infection | 1 | Patient |
| 2024 | Under-Sensing | 1 | Device |
| 2024 | Signal Artifact/Noise | 2 | Device |
| 2024 | Over-Sensing | 3 | Device |
| 2024 | Low impedance | 1 | Device |
| 2024 | Inappropriate/Inadequate Shock/Stimulation | 3 | Device |
| 2024 | Fracture | 1 | Device |
| 2024 | Failure to Read Input Signal | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2023 | Undesired Nerve Stimulation | 1 | Patient |
| 2023 | Shock from Patient Lead(s) | 3 | Patient |
| 2023 | Electric Shock | 6 | Patient |
| 2023 | Under-Sensing | 1 | Device |
| 2023 | Signal Artifact/Noise | 1 | Device |
| 2023 | Premature Discharge of Battery | 2 | Device |
| 2023 | Over-Sensing | 6 | Device |
| 2023 | No Apparent Adverse Event | 1 | Device |
| 2023 | Migration | 1 | Device |
| 2023 | Malposition of Device | 1 | Device |
| 2023 | Low impedance | 1 | Device |
| 2023 | Inappropriate/Inadequate Shock/Stimulation | 8 | Device |
| 2023 | High impedance | 2 | Device |
| 2023 | Fracture | 1 | Device |
| 2023 | Failure to Read Input Signal | 3 | Device |
| 2023 | Failure to Convert Rhythm | 1 | Device |
| 2023 | Defective Device | 1 | Device |
| 2023 | Data Problem | 1 | Device |
| 2023 | Connection Problem | 2 | Device |
| 2023 | Battery Problem | 3 | Device |
| 2022 | Signal Artifact/Noise | 3 | Device |
| 2022 | Premature Discharge of Battery | 4 | Device |
| 2022 | Over-Sensing | 5 | Device |
| 2022 | Noise, Audible | 1 | Device |
| 2022 | Incorrect, Inadequate or Imprecise Result or Readings | 2 | Device |
| 2022 | Inappropriate/Inadequate Shock/Stimulation | 3 | Device |
| 2022 | High impedance | 3 | Device |
| 2022 | Failure to Read Input Signal | 3 | Device |
| 2022 | Failure to Charge | 1 | Device |
| 2022 | Difficult to Remove | 2 | Device |
| 2022 | Delayed Charge Time | 2 | Device |
| 2022 | Connection Problem | 5 | Device |
| 2022 | Battery Problem | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2021 | Defective Device | 3 | Device |
| 2020 | Insufficient Information | 2 | Patient |
| 2020 | Connection Problem | 2 | Device |
| 2020 | Battery Problem | 1 | Device |