BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1853726 · Received September 29, 2010

    Report

    Report Number
    1824206-2010-10203
    Event Type
    Malfunction
    Date Received
    September 29, 2010
    Date of Event
    September 3, 2010
    Report Date
    September 3, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND A SCREW MISSING FROM THE HEX ROD. THE TECHNICIAN INSTALLED A NEW HEX ROD SCREW TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE BRAKE WILL ENGAGE BUT DOES NOT HOLD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1