BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3071307 · Received April 9, 2013

    Report

    Report Number
    1824206-2013-02041
    Event Type
    Malfunction
    Date Received
    April 9, 2013
    Date of Event
    March 13, 2013
    Report Date
    March 13, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    RI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE SIDE RAIL IS MISSING THE LATCH BOLT AND NUT. THE ACCOUNT REPLACED THE SIDE RAIL LATCH BOLT AND NUT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE SIDE RAIL IS NOT LATCHING. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    147791 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8050

    Patients

    Seq Age Sex Outcome Treatment
    1