IMPLANTABLE TACHY LEAD
This device is manufactured by BOSTON SCIENTIFIC, MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT, MEDTRONIC PLC, MEDTRONIC PUERTO RICO, MEDTRONIC PUERTO RICO OPERATIONS CO and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Over-Sensing | 1 | Device |
| 2024 | Impedance Problem | 1 | Device |
| 2024 | High impedance | 3 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Decreased Sensitivity | 1 | Device |
| 2023 | Unspecified Infection | 1 | Patient |
| 2023 | Syncope/Fainting | 1 | Patient |
| 2023 | Shock from Patient Lead(s) | 1 | Patient |
| 2023 | Erosion | 1 | Patient |
| 2023 | Chest Pain | 1 | Patient |
| 2023 | Under-Sensing | 1 | Device |
| 2023 | Signal Artifact/Noise | 1 | Device |
| 2023 | Pacing Problem | 1 | Device |
| 2023 | Over-Sensing | 2 | Device |
| 2023 | Inappropriate/Inadequate Shock/Stimulation | 1 | Device |
| 2023 | High impedance | 2 | Device |
| 2023 | Fracture | 1 | Device |
| 2023 | Device Sensing Problem | 1 | Device |
| 2023 | Connection Problem | 1 | Device |
| 2023 | Appropriate Term/Code Not Available | 2 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2022 | Shock from Patient Lead(s) | 1 | Patient |
| 2022 | Signal Artifact/Noise | 3 | Device |
| 2022 | Over-Sensing | 4 | Device |
| 2022 | Mechanical Problem | 1 | Device |
| 2022 | Inappropriate/Inadequate Shock/Stimulation | 2 | Device |
| 2022 | Impedance Problem | 1 | Device |
| 2022 | High impedance | 1 | Device |
| 2022 | High Capture Threshold | 1 | Device |
| 2022 | Fracture | 1 | Device |
| 2022 | Device-Device Incompatibility | 1 | Device |