BEUDAMED
    FDA Adverse Event Death Summary report: N

    POWER X1

    MDR report key: 19775873 · Received July 18, 2024

    Report

    Report Number
    1523574-2024-00055
    Event Type
    Death
    Date Received
    July 18, 2024
    Date of Event
    June 25, 2024
    Report Date
    July 18, 2024
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    UDI-DI
    00190790002183
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED THE STRETCHER WAS INVOLVED IN A MOTOR VEHICLE ACCIDENT WHILE TRANSPORTING AN EMERGENCY PATIENT. THE AMBULANCE WAS STRUCK BY ANOTHER VEHICLE AND OVERTURNED. THE PATIENT WAS REPORTED DECEASED AND TWO MEMBERS OF THE MEDIC CREW WERE INJURED. THERE WAS NO ALLEGATION OF THE STRETCHER BEING A CONTRIBUTING FACTOR TO THE PATIENT CONDITION NOR HAS THERE BEEN ALLEGATION OF PRODUCT MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1905687 POWER X1 POWER X1 FPO FERNO-WASHINGTON, INC. 0015807 00190790002183

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other| D