BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MULTIRALL

    MDR report key: 3601929 · Received December 2, 2013

    Report

    Report Number
    1824206-2013-05429
    Event Type
    Malfunction
    Date Received
    December 2, 2013
    Date of Event
    October 31, 2013
    Report Date
    October 31, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COMPLAINT RECORD ALLEGES THAT WHILE LIFTING A PATIENT THE QRH SLING BAR ON THE MULTIRALL DETACHED. NO PATIENT IMPACT. REFERENCE MFR REPORT 8030916-2013-00090.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    623931 MULTIRALL NON-AC POWERED PATIENT LIFT FSA LIKO AB MULTIRALL 200

    Patients

    Seq Age Sex Outcome Treatment
    1