BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1952435 · Received January 3, 2011

    Report

    Report Number
    1824206-2011-00002
    Event Type
    Malfunction
    Date Received
    January 3, 2011
    Date of Event
    December 12, 2010
    Report Date
    December 12, 2010
    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

    TECHNICIAN FOUND THE SCREW MISSING FROM THE SIDE RAIL SHOULDER LATCH KEEPING THE SIDE RAIL FROM LOCKING IN UP POSITION. THE TECHNICIAN REPLACED THE SHOULDER LATCH BOLT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED THAT THE SIDE RAIL WOULD NOT LOCK IN THE UP POSITION. NO PT 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