BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 3224721 · Received July 3, 2013

    Report

    Report Number
    1824206-2013-03341
    Event Type
    Malfunction
    Date Received
    July 3, 2013
    Date of Event
    June 7, 2013
    Report Date
    June 7, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NZ
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SINGLE FAULT SAFETY DRUM LEAKING OIL. MFR REF # 8030916-2013-00040.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    304655 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB LIKORALL 242 S

    Patients

    Seq Age Sex Outcome Treatment
    1