BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1952684 · Received January 4, 2011

    Report

    Report Number
    1824206-2011-00034
    Event Type
    Malfunction
    Date Received
    January 4, 2011
    Date of Event
    December 14, 2010
    Report Date
    December 14, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE PT LEFT SIDE RAIL WILL NOT LATCH BECAUSE THE END TUBE IS BROKEN OFF OF THE SIDE RAIL. THE TECHNICIAN REPLACED THE PT LEFT END TUBE AND INSTALLED RATCHET RIVETS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED THAT THE SIDE RAIL WILL NOT LATCH. NO ALLEGED INJURY BY ACCOUNT.

    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