IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
This device is manufactured by ST JUDE MEDICAL, ST JUDE MEDICAL (CRM-SUNNYVALE), ST JUDE MEDICAL (CRM-SYLMAR), ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION, ST JUDE MEDICAL IRVINE and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Unspecified Infection | 1 | Patient |
| 2024 | Insufficient Information | 1 | Patient |
| 2024 | No Apparent Adverse Event | 1 | Device |
| 2024 | Defibrillation/Stimulation Problem | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2023 | Insufficient Information | 1 | Patient |
| 2023 | Inappropriate or Unexpected Reset | 1 | Device |
| 2023 | Environmental Compatibility Problem | 1 | Device |
| 2023 | Defective Device | 1 | Device |
| 2022 | Premature Discharge of Battery | 3 | Device |
| 2022 | Inappropriate or Unexpected Reset | 1 | Device |
| 2022 | Defective Device | 1 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2021 | Premature Discharge of Battery | 2 | Device |
| 2020 | Premature Discharge of Battery | 4 | Device |
| 2020 | Failure to Interrogate | 1 | Device |