BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FERNO POWERFLEXX STRETCHER

    MDR report key: 2492232 · Received March 12, 2012

    Report

    Report Number
    1523574-2012-00002
    Event Type
    Injury
    Date Received
    March 12, 2012
    Date of Event
    January 15, 2012
    Report Date
    March 12, 2012
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    MANUFACTURER'S REPRESENTATIVE INSPECTED PRODUCT AT USER'S FACILITY. FINDINGS INCLUDED MISALIGNED/LOOSE CHARGING SYSTEMS, LOOSE POWERPACS AND IMPROPERLY ADJUSTED MANUAL RELEASE CABLE. MANUFACTURER HAS REQUESTED THE PRODUCT BE RETURNED FOR FURTHER EVALUATION. MANUFACTURER'S INVESTIGATION CONTINUES.

    Description of Event or Problem · 1

    POWER STRETCHER OPERATED CORRECTLY WHILE BEING UNLOADED FROM THE AMBULANCE, PATIENT RETRIEVAL AND TRANSPORT TO THE AMBULANCE FOR LOADING. STRETCHER HAD NO POWER UPON EMTS TRYING TO ACTIVATE FOR LOAD. ONE EMT EXPERIENCED A BACK STRAIN UPON TRYING TO LOAD THE PATIENT MANUALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FERNO POWERFLEXX STRETCHER FERNO POWERFLEXX STRETCHER FPO FERNO-WASHINGTON, INC. POWERFLEXX

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Other