BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONTOURA 1000 / 1080

    MDR report key: 3832495 · Received April 21, 2014

    Report

    Report Number
    1419652-2014-00108
    Event Type
    Injury
    Date Received
    April 21, 2014
    Date of Event
    February 11, 2014
    Report Date
    March 24, 2014
    Manufacturer
    ARJOHUNTLEIGH POLSKA SP. Z.O.O.
    Product Code
    OSI
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN INDICATED BY THE CUSTOMER THAT "WHILST SEVERAL PEOPLE ATTEMPTING TO MOVE PATIENT ON BARIATRIC BED THE BRAKES FAILED CAUSING BED TO MOVE AND TRAPPING A NURSE AT THE HEAD END OF THE BED, HER KNEE WAS PINNED UNDER THE BED FRAME UNTIL BED WAS MOVED BACK IN POSITION." REF MFR REPORT 3007420694-2014-00048.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    241265 CONTOURA 1000 / 1080 OSI ARJOHUNTLEIGH POLSKA SP. Z.O.O. C1000

    Patients

    Seq Age Sex Outcome Treatment
    1 Other