BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2031851 · Received March 21, 2011

    Report

    Report Number
    1824206-2011-01713
    Event Type
    Malfunction
    Date Received
    March 21, 2011
    Date of Event
    March 2, 2011
    Report Date
    March 2, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT AFTER BRAKE/STEER PEDAL HAS BEEN SET TO BRAKE POSITION, STRETCHER WOULD STILL ROLLS. ADJUSTED BRAKE POSITION FOR ALL FOUR CASTERS. FOUND BROKEN SCREW IN HEAD AND FOOT HEX RODS. REPLACED BOTH HEX RODS TO RESOLVE THIS ISSUE. STRETCHER FOUND ER.

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT AFTER BRAKE/STEER PEDAL HAS BEEN SET TO BRAKE POSITION, STRETCHER STILL ROLLS. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P8000

    Patients

    Seq Age Sex Outcome Treatment
    1