BEUDAMED
    FDA Adverse Event Other Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3143235 · Received May 31, 2013

    Report

    Report Number
    1824206-2013-02923
    Event Type
    Other
    Date Received
    May 31, 2013
    Date of Event
    May 2, 2013
    Report Date
    May 2, 2013
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME. A FOLLOW UP REPORT WILL BE SENT ONCE THE INVESTIGATION IS COMPLETED FOR THE INJURY.

    Description of Event or Problem · 1

    THE NURSE ALLEGED THAT THE BRAKE IS DIFFICULT TO ACCESS AND ALSO THAT THE BRAKE IS VERY HARD TO ACTIVATE WITH THE FOOT WHICH RESULTED IN A VERY SMALL FRACTURE ON HER FOOT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    241346 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1 Other