AED
This device is manufactured by PHILIPS MEDICAL SYSTEMS, PHILIPS MEDICAL SYSTEMS (HTST RETURNS), PHILIPS NORTH AMERICA.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Cardiac Arrest | 1 | Patient |
| 2024 | No Audible Prompt/Feedback | 1 | Device |
| 2024 | Inaudible or Unclear Audible Prompt/Feedback | 5 | Device |
| 2024 | Failure to Deliver Shock/Stimulation | 1 | Device |
| 2024 | Failure of Device to Self-Test | 20 | Device |
| 2024 | Audible Prompt/Feedback Problem | 1 | Device |
| 2023 | Cardiac Arrest | 1 | Patient |
| 2023 | Unintended Power Up | 1 | Device |
| 2023 | Incorrect, Inadequate or Imprecise Result or Readings | 1 | Device |
| 2023 | Inaudible or Unclear Audible Prompt/Feedback | 9 | Device |
| 2023 | Inappropriate/Inadequate Shock/Stimulation | 1 | Device |
| 2023 | Inappropriate Audible Prompt/Feedback | 2 | Device |
| 2023 | Failure to Deliver Shock/Stimulation | 1 | Device |
| 2023 | Failure of Device to Self-Test | 39 | Device |
| 2023 | Audible Prompt/Feedback Problem | 3 | Device |
| 2022 | No Audible Prompt/Feedback | 8 | Device |
| 2022 | Inaudible or Unclear Audible Prompt/Feedback | 20 | Device |
| 2022 | Inappropriate Audible Prompt/Feedback | 1 | Device |
| 2022 | Failure to Power Up | 1 | Device |
| 2022 | Failure of Device to Self-Test | 28 | Device |
| 2022 | Display or Visual Feedback Problem | 1 | Device |
| 2021 | Premature Discharge of Battery | 1 | Device |
| 2021 | Output Problem | 2 | Device |
| 2021 | No Audible Alarm | 1 | Device |
| 2021 | Inaudible or Unclear Audible Prompt/Feedback | 4 | Device |
| 2021 | Defective Device | 5 | Device |
| 2021 | Battery Problem | 1 | Device |