AUTOMATED EXTERNAL DEFIBRILLATOR
This device is manufactured by DEFIBTECH.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Unspecified Heart Problem | 3 | Patient |
2024 | Cardiac Arrest | 1 | Patient |
2024 | Use of Device Problem | 2 | Device |
2024 | Premature Discharge of Battery | 2 | Device |
2024 | Power Problem | 1 | Device |
2024 | Physical Resistance/Sticking | 1 | Device |
2024 | No Visual Prompts/Feedback | 1 | Device |
2024 | No Audible Prompt/Feedback | 17 | Device |
2024 | Moisture Damage | 1 | Device |
2024 | Mechanical Problem | 2 | Device |
2024 | Mechanical Jam | 2 | Device |
2024 | Insufficient Information | 6 | Device |
2024 | Inaudible or Unclear Audible Prompt/Feedback | 1 | Device |
2024 | Improper or Incorrect Procedure or Method | 1 | Device |
2024 | Failure to Power Up | 228 | Device |
2024 | Failure to Eject | 1 | Device |
2024 | Failure to Charge | 1 | Device |
2024 | Energy Output Problem | 1 | Device |
2024 | Electrical /Electronic Property Problem | 10 | Device |
2024 | Display or Visual Feedback Problem | 2 | Device |
2024 | Difficult to Open or Close | 1 | Device |
2024 | Crack | 1 | Device |
2024 | Connection Problem | 4 | Device |
2024 | Break | 1 | Device |
2024 | Battery Problem | 52 | Device |
2024 | Audible Prompt/Feedback Problem | 2 | Device |
2023 | Unspecified Heart Problem | 2 | Patient |
2023 | Cardiac Arrest | 1 | Patient |
2023 | Mechanical Problem | 2 | Device |
2023 | Incomplete or Inadequate Connection | 1 | Device |
2023 | Failure to Power Up | 39 | Device |
2023 | Connection Problem | 2 | Device |
2022 | Unspecified Heart Problem | 1 | Patient |
2022 | Mechanical Problem | 2 | Device |
2022 | Intermittent Loss of Power | 1 | Device |
2022 | Failure to Deliver Shock/Stimulation | 1 | Device |
2019 | Power Problem | 1 | Device |
2019 | Mechanical Problem | 1 | Device |
2019 | Failure to Power Up | 4 | Device |
2019 | Failure to Deliver Shock/Stimulation | 1 | Device |
2019 | Failure to Analyze Signal | 1 | Device |
2019 | Complete Loss of Power | 1 | Device |
2019 | Charging Problem | 1 | Device |
2018 | Moisture Damage | 1 | Device |
2018 | Failure to Run on Battery | 1 | Device |
2018 | Failure to Power Up | 1 | Device |
2018 | Failure to Deliver Shock/Stimulation | 1 | Device |
2018 | Failure to Analyze Signal | 1 | Device |
2018 | Device Operates Differently Than Expected | 8 | Device |
2018 | Defibrillation/Stimulation Problem | 2 | Device |
2018 | Battery Problem | 2 | Device |
2017 | Therapy Delivered to Incorrect Body Area | 1 | Device |
2017 | Premature Discharge of Battery | 1 | Device |
2017 | Overheating of Device | 1 | Device |
2017 | Loss of Power | 1 | Device |
2017 | Image Display Error/Artifact | 1 | Device |
2017 | Failure To Service | 1 | Device |
2017 | Device Stops Intermittently | 1 | Device |
2017 | Device Operates Differently Than Expected | 13 | Device |
2017 | Device Maintenance Issue | 1 | Device |
2017 | Device Displays Incorrect Message | 5 | Device |
2017 | Battery Problem | 1 | Device |
2017 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2016 | No Display/Image | 1 | Device |
2016 | Moisture or Humidity Problem | 1 | Device |
2016 | Low Battery | 1 | Device |
2016 | Inappropriate/Inadequate Shock/Stimulation | 1 | Device |
2016 | Failure to Power Up | 2 | Device |
2016 | Device Operates Differently Than Expected | 2 | Device |
2016 | Device Expiration Issue | 1 | Device |
2016 | Device Displays Incorrect Message | 2 | Device |
2016 | Defibrillation/Stimulation Problem | 4 | Device |