BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LIKORALL

    MDR report key: 3234180 · Received July 10, 2013

    Report

    Report Number
    1824206-2013-03427
    Event Type
    Injury
    Date Received
    July 10, 2013
    Date of Event
    June 14, 2013
    Report Date
    June 17, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING TRANSFER OF A CHILD IN A SLING THE QRH ON THE SLING BAR DETACHED FROM THE LIFT STRAP DROPPING THE CHILD TO THE FLOOR. SHOCK AND BRUISING ON LEFT CHEEK ALLEGED. REFERENCE MFR REPORT # 8030916-2013-00045.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    318239 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB LIKORALL 200

    Patients

    Seq Age Sex Outcome Treatment
    1