BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OBGYN TRANSTAR TRANSTAR FRAME OB/G

    MDR report key: 1730615 · Received December 23, 2009

    Report

    Report Number
    1824206-2009-07894
    Event Type
    Malfunction
    Date Received
    December 23, 2009
    Date of Event
    December 5, 2009
    Report Date
    December 5, 2009
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN REPLACED THE CYLINDER AND THIS REPAIRED THE STRETCHER. THE CAUSE WAS UNKNOWN.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE HI/LOW WAS DRIFTING DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OBGYN TRANSTAR TRANSTAR FRAME OB/G WHEELED STRETCHER FPO HILL-ROM RITTER P8050G000091

    Patients

    Seq Age Sex Outcome Treatment
    1