DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATIO
This device is manufactured by MEDTRONIC, MEDTRONIC MED REL MEDTRONIC PUERTO RICO, MEDTRONIC PUERTO RICO, MEDTRONIC PUERTO RICO OPERATIONS CO.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Tachycardia | 2 | Patient |
| 2024 | Syncope/Fainting | 1 | Patient |
| 2024 | Shock from Patient Lead(s) | 3 | Patient |
| 2024 | Insufficient Information | 1 | Patient |
| 2024 | Fall | 1 | Patient |
| 2024 | Dizziness | 1 | Patient |
| 2024 | Chest Pain | 1 | Patient |
| 2024 | Bradycardia | 1 | Patient |
| 2024 | Premature Discharge of Battery | 1 | Device |
| 2024 | Pacing Problem | 1 | Device |
| 2024 | Mechanical Problem | 1 | Device |
| 2024 | Inappropriate/Inadequate Shock/Stimulation | 2 | Device |
| 2024 | Failure to Deliver Shock/Stimulation | 1 | Device |
| 2024 | Device Sensing Problem | 3 | Device |
| 2024 | Device Dislodged or Dislocated | 1 | Device |
| 2023 | Unspecified Infection | 1 | Patient |
| 2023 | Tachycardia | 1 | Patient |
| 2023 | Shock from Patient Lead(s) | 3 | Patient |
| 2023 | Bradycardia | 1 | Patient |
| 2023 | Signal Artifact/Noise | 1 | Device |
| 2023 | Premature Discharge of Battery | 2 | Device |
| 2023 | Pacing Problem | 2 | Device |
| 2023 | Over-Sensing | 1 | Device |
| 2023 | Inappropriate/Inadequate Shock/Stimulation | 3 | Device |
| 2023 | Failure to Deliver Shock/Stimulation | 1 | Device |
| 2023 | Electromagnetic Interference | 1 | Device |
| 2023 | Device Sensing Problem | 4 | Device |
| 2023 | Appropriate Term/Code Not Available | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2022 | Unspecified Infection | 1 | Patient |
| 2022 | Syncope/Fainting | 1 | Patient |
| 2022 | Fall | 1 | Patient |
| 2022 | Discomfort | 1 | Patient |
| 2022 | Bradycardia | 1 | Patient |
| 2022 | Signal Artifact/Noise | 1 | Device |
| 2022 | Premature Discharge of Battery | 4 | Device |
| 2022 | Pacing Problem | 3 | Device |
| 2022 | Over-Sensing | 2 | Device |
| 2022 | Misconnection | 1 | Device |
| 2022 | Inappropriate/Inadequate Shock/Stimulation | 2 | Device |
| 2022 | High impedance | 1 | Device |
| 2022 | Failure to Interrogate | 1 | Device |
| 2022 | Electromagnetic Interference | 2 | Device |
| 2022 | Device Sensing Problem | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
| 2021 | Unspecified Infection | 1 | Patient |
| 2021 | Thrombosis/Thrombus | 1 | Patient |
| 2021 | Insufficient Information | 1 | Patient |
| 2021 | Drug Resistant Bacterial Infection | 1 | Patient |
| 2021 | Premature Discharge of Battery | 1 | Device |
| 2021 | High impedance | 1 | Device |
| 2021 | Appropriate Term/Code Not Available | 1 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 2 | Device |