BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 2243512 · Received August 19, 2011

    Report

    Report Number
    8030916-2011-00056
    Event Type
    Malfunction
    Date Received
    August 19, 2011
    Date of Event
    July 28, 2011
    Report Date
    July 28, 2011
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    PARTS ARE BEING RETURNED TO MFR FOR FURTHER ANALYSIS.

    Description of Event or Problem · 1

    FACILITY ALLEGED THAT THE E-CARD IN THE LIKORALL MOTOR WAS SPARKING HEAVILY AND THAT THE IRC TAPE WAS BURNT IN THE SECONDARY RAIL. NO INJURY ALLEGED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1