BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VIKING

    MDR report key: 3233753 · Received July 8, 2013

    Report

    Report Number
    1824206-2013-03389
    Event Type
    Malfunction
    Date Received
    July 8, 2013
    Report Date
    June 14, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CENTER BOLT ON A UNIVERSAL SLING BAR BROKE DURING TRANSFER OF A PT. NO INJURY ALLEGED. REF MFR # 8030916-2013-00043.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    309340 VIKING NON-AC POWERED PATIENT LIFT FSA LIKO AB VIKING M

    Patients

    Seq Age Sex Outcome Treatment
    1