BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2053571 · Received March 17, 2011

    Report

    Report Number
    1824206-2011-01674
    Event Type
    Malfunction
    Date Received
    March 17, 2011
    Date of Event
    February 28, 2011
    Report Date
    February 28, 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 THE STRETCHER WOULD STILL ROLL AFTER PEDAL IS PUT INTO BRAKE POSITION. ADJUSTED THE BRAKE POSITION FOR ALL FOUR CASTERS TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE STRETCHER WOULD STILL ROLL AFTER PEDAL IS PUT INTO BRAKE POSITION.

    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