BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNO

    MDR report key: 2980099 · Received February 20, 2013

    Report

    Report Number
    8030916-2013-00010
    Event Type
    Malfunction
    Date Received
    February 20, 2013
    Date of Event
    January 22, 2013
    Report Date
    January 22, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COMPLAINT RECORD STATES THAT THE CHARGING CABLE IS SHORT-CIRCUITED AT THE WALL PLUG. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    74193 UNO NON-AC POWERED PATIENT LIFT FSA LIKO AB UNO

    Patients

    Seq Age Sex Outcome Treatment
    1