BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOLVO 7007 ES

    MDR report key: 3913248 · Received June 27, 2014

    Report

    Report Number
    1824206-2014-01864
    Event Type
    Malfunction
    Date Received
    June 27, 2014
    Date of Event
    June 4, 2014
    Report Date
    June 4, 2014
    Manufacturer
    LIKO, AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO HILL-ROM THAT THE LEFT LEG OF THE LIFT WAS SLIDING IN AND OUT BY ITSELF. NO INJURY ALLEGED. MFR - 8030916-2014-00046.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    376057 GOLVO 7007 ES NON-AC POWERED PATIENT LIFT FSA LIKO, AB 20000010

    Patients

    Seq Age Sex Outcome Treatment
    1