BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR FRAME OB/G

    MDR report key: 2401625 · Received November 30, 2011

    Report

    Report Number
    1824206-2011-05985
    Event Type
    Malfunction
    Date Received
    November 30, 2011
    Date of Event
    November 4, 2011
    Report Date
    November 4, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    BED HAS BEEN PICKED UP FOR REPAIR BY A THIRD PARTY. REPAIR IS NOT YET CONFIRMED.

    Description of Event or Problem · 1

    FACILITY ALLEGED THAT THE SIDERAIL LATCH WAS NOT WORKING ON THE STRETCHER. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR FRAME OB/G WHEELED STRETCHER FPO HILL-ROM, INC. P8050

    Patients

    Seq Age Sex Outcome Treatment
    1