BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 3130460 · Received March 26, 2013

    Report

    Report Number
    8030916-2013-00018
    Event Type
    Malfunction
    Date Received
    March 26, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IS AN INITIAL REPORT. A SUPPLEMENTARY REPORT WILL BE FILED WHEN THE SLING BAR IS RETURNED TO THE MANUFACTURER FOR EVALUATION.

    Description of Event or Problem · 1

    REFERENCE TO IMPORTER REPORT # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    125408 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB

    Patients

    Seq Age Sex Outcome Treatment
    1