BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 3653620 · Received January 29, 2014

    Report

    Report Number
    1824206-2014-00251
    Event Type
    Malfunction
    Date Received
    January 29, 2014
    Date of Event
    January 13, 2014
    Report Date
    January 13, 2014
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SAFETY DRUM LEAKING OIL. NO INJURY ALLEGED. REFERENCE MFR REPORT 8030916-2014-00005.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    62243 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB LIKORALL 242 S

    Patients

    Seq Age Sex Outcome Treatment
    1