BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MULTIRALL 200

    MDR report key: 2900227 · Received November 13, 2012

    Report

    Report Number
    8030916-2012-00102
    Event Type
    Malfunction
    Date Received
    November 13, 2012
    Date of Event
    October 23, 2012
    Report Date
    October 23, 2012
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT STATED THAT THEY COULD RECREATE THE ISSUE WHEN RUNNING THE LIFT EITHER UP OR DOWN WITH A 170 LB LOAD. THEY TESTED THE MULTIRAIL, BOTH RIGHT SIDE UP AND UPSIDE DOWN AND FOUND THE LIFT STRAP WAS TWISTED AROUND THE DRUM ALLOWING IT TO SLIP. THE STRAP WAS FULLY EXTENDED AND TESTED AGAIN WITH NO JERK OR BUMP IN THE LIFT. THE LIFT WAS RETURNED TO SERVICE.

    Description of Event or Problem · 1

    THE COMPLAINANT STATED THAT THE LIFT DROPPED 6-8 INCHES WITH A PT IN THE LIFT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MULTIRALL 200 LIFT, PATIENT, NON-AC-POWERED FSA LIKO AB 3130001

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK