BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FERNO

    MDR report key: 11884926 · Received May 25, 2021

    Report

    Report Number
    MW5101531
    Event Type
    Injury
    Date Received
    May 25, 2021
    Date of Event
    February 8, 2021
    Report Date
    May 21, 2021
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Report Source
    Voluntary report
    Reporter Location
    KY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    FERNO STRETCHER USED TO TRANSPORT PATIENT HAS A SAFETY STRAP TO GO OVER PATIENTS¿ LOWER LEGS. IF NOT PLACED TO PRIOR TO STRETCHER MOVEMENT, THERE IS A POTENTIAL FOR THE STRAP TO GET CAUGHT IN THE UNDER CARRIAGE OF THE STRETCHER. THIS COULD APPLY EXCESSIVE PRESSURE TO THE PATIENT¿S LOWER LEGS. AMBULANCE STAFF DID A TEST TO RECREATE WHAT OCCURRED. UNABLE TO RECREATE EVENT. FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    772822 FERNO STRETCHER, WHEELED FPO FERNO-WASHINGTON, INC. FERNO POWER FLEXX

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization