BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 3130539 · Received March 25, 2013

    Report

    Report Number
    1824206-2013-01640
    Event Type
    Malfunction
    Date Received
    March 25, 2013
    Date of Event
    February 20, 2013
    Report Date
    February 20, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SAFETY DRUM LEAKING OIL. NO INJURY ALLEGED. REFERENCE MANUFACTURER REPORT NUMBER 8030916-2013-00016.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    122909 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB LIKORALL 250 ES

    Patients

    Seq Age Sex Outcome Treatment
    1