BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SABINA

    MDR report key: 3233781 · Received July 10, 2013

    Report

    Report Number
    1824206-2013-03428
    Event Type
    Malfunction
    Date Received
    July 10, 2013
    Date of Event
    June 24, 2013
    Report Date
    June 24, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    MAST WELD BROKE WHERE LEG SUPPORT ATTACHES TO SABINA II LIFT. NO INJURY ALLEGED. REF MFR # 8030916-2013-00046.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    316467 SABINA NON-AC POWERED PATIENT LIFT FSA LIKO AB SABINA II

    Patients

    Seq Age Sex Outcome Treatment
    1