BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 1945978 · Received December 17, 2010

    Report

    Report Number
    8030916-2010-00068
    Event Type
    Malfunction
    Date Received
    December 17, 2010
    Date of Event
    January 1, 2009
    Report Date
    April 7, 2009
    Manufacturer
    LIKO AB
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THIS MDR IS PART OF A RETROSPECTIVE REVIEW IN ACCORDANCE WITH CAPA ACTIVITIES.

    Description of Event or Problem · 1

    A CARE GIVER ATTACHED THE SLINGBAR WITH QUICK RELEASE HOOK TO THE HANDCONTROL HANGER INSTEAD OF TO THE Q-LINK. WHEN THE PT WAS LIFTED, THE HAND CONTROL HANGER BECAME DETACHED AND THE PT FELL TO THE FLOOR.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1