BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 3692898 · Received March 11, 2014

    Report

    Report Number
    1824206-2014-00799
    Event Type
    Malfunction
    Date Received
    March 11, 2014
    Date of Event
    February 13, 2014
    Report Date
    February 13, 2014
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INTERMITTENT FUNCTION OF THE EMERGENCY STOP. NO PATIENT IMPACT. REFERENCE MFR REPORT 8030916-2014-00018.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    144918 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB LIKORALL 242 S R2R

    Patients

    Seq Age Sex Outcome Treatment
    1