BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1970432 · Received January 18, 2011

    Report

    Report Number
    1824206-2011-00253
    Event Type
    Malfunction
    Date Received
    January 18, 2011
    Date of Event
    October 23, 2006
    Report Date
    October 23, 2006
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE SIDE RAIL SHOULDER BOLT TO RESOLVE THE ISSUE. THIS MDR IS A RESULT OF CAPA ACTIVITY FOR THE RETROSPECTIVE REVIEW OF COMPLAINTS.

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED THAT THE SIDE RAIL WILL NOT LATCH INTO PLACE WHEN RAISED. NO PATIENT IMPACT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1