BEUDAMED
    FDA Adverse Event Death Summary report: N

    POWER F2

    MDR report key: 24689746 · Received March 25, 2026

    Report

    Report Number
    1523574-2026-00029
    Event Type
    Death
    Date Received
    March 25, 2026
    Report Date
    March 25, 2026
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    UDI-DI
    00190790006570
    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 HAD TO BE MANUALLY LOWERED BUT THEN THE CARRIAGE ARMS WOULD NOT LOWER DOWNWARD TO RELEASE THE STRETCHER FROM THE LOADER. THE CREW WAS ABLE TO MANUALLY LOWER THE CARRIAGE ARMS AND COMPLETE THE TRANSPORT INTO THE HOSPITAL. THE END USER ADVISED 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 THEY WERE UNABLE TO DUPLICATE THE ISSUE AFER THE INCIDENT AND MADE THE DECISION TO KEEP THE POWER F2 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
    532118 POWER F2 POWER F2 FPO FERNO-WASHINGTON, INC. 0567093 M255240 00190790006570

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male Death