BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SABINA

    MDR report key: 3224691 · Received July 3, 2013

    Report

    Report Number
    1824206-2013-03340
    Event Type
    Malfunction
    Date Received
    July 3, 2013
    Date of Event
    December 6, 2012
    Report Date
    December 6, 2012
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CRACK IN THE FOOT TRAY ON A SABINA II LIFT. NO INJURY ALLEGED. MFR REF # 8030916-2013-00039.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    304652 SABINA NON-AC POWERED PATIENT LIFT FSA LIKO AB SABINA II

    Patients

    Seq Age Sex Outcome Treatment
    1