BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNO

    MDR report key: 2990098 · Received February 21, 2013

    Report

    Report Number
    8030916-2013-00011
    Event Type
    Malfunction
    Date Received
    February 21, 2013
    Date of Event
    January 23, 2012
    Report Date
    January 23, 2012
    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 ACTUATOR BENT DURING WEIGHT TESTING. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    75430 UNO NON-AC POWERED PATIENT LIFT FSA LIKO AB UNO 102 EE

    Patients

    Seq Age Sex Outcome Treatment
    1