BEUDAMED
    FDA Adverse Event Death Summary report: N

    POWER X2

    MDR report key: 24689745 · Received March 25, 2026

    Report

    Report Number
    1523574-2026-00028
    Event Type
    Death
    Date Received
    March 25, 2026
    Report Date
    March 25, 2026
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    UDI-DI
    00190790003210
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE END USER REPORTED AFTER ARRIVAL AT THE HOSPITAL WITH AN ACTIVE CARDIAC PATIENT, WHILE UNLOADING THE STRETCHER FROM THE AMBULANCE, THE LEGS OF THE STRETCHER WOULD NOT LOWER UNDER POWER USING THE BUTTONS ON THE STRETCHER. THE MANUAL RELEASE OPTION WAS UTILIZED TO LOWER THE LEGS AND COMPLETE THE TRANSPORT INTO THE HOSPITAL. THE END USER ADVISED THAT AN ESTIMATED TWO-MINUTE DELAY WAS EXPERIENCED DURING THE UNLOADING PROCESS. PATIENT DETAILS: MALE, APPROXIMATELY 220 LBS, PATIENT WAS EXPERIENCING AND BEING TREATED FOR CARDIAC ARREST ON SCENE AND THROUGHOUT TRANSPORT. CPR WAS BEING ADMINISTERED VIA LIFELINE ARM. THE PATIENT WAS LATER PRONOUNCED DECEASED AT THE HOSPITAL. THE END USER ADVISED THAT THEY EVALUATED THE STRETCHER THE NEXT DAY AND WERE UNABLE TO DUPLICATE THE REPORTED ISSUE AND MADE THE DECISION TO KEEP THE STRETCHER IN SERVICE, IN MANUAL MODE ONLY, UNTIL EVALUATION. THIS CONTINUES TO BE AN ACTIVE INVESTIGATION AND ADDITIONAL INFORMATION WILL BE PROVIDED IN A FOLLOW UP REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    532117 POWER X2 POWER X2 FPO FERNO-WASHINGTON, INC. 0015816 M260530 00190790003210

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male Death