BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2944223 · Received January 10, 2013

    Report

    Report Number
    1824206-2013-00283
    Event Type
    Malfunction
    Date Received
    January 10, 2013
    Date of Event
    December 29, 2012
    Report Date
    December 29, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE SIDE RAIL LATCH PLATE AND PIVOT BOLT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

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

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    14193 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1