BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2843756 · Received October 26, 2012

    Report

    Report Number
    1824206-2012-06868
    Event Type
    Malfunction
    Date Received
    October 26, 2012
    Date of Event
    October 9, 2012
    Report Date
    October 9, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NM, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE SIDE RAIL PLATE BENT AND THE SIDE RAIL SCREW BOLT IS MISSING. THE TECHNICIAN REPLACED THE SIDE RAIL PLATE AND SIDE RAIL SCREW BOLT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE SIDE RAIL WILL NOT LATCH. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8050

    Patients

    Seq Age Sex Outcome Treatment
    1