BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CIRRUS

    MDR report key: 6921879 · Received October 6, 2017

    Report

    Report Number
    6921879
    Event Type
    Malfunction
    Date Received
    October 6, 2017
    Date of Event
    September 8, 2017
    Report Date
    September 20, 2017
    Manufacturer
    TOLLOS
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    DE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CEILING LIFT FAILED WHILE LIFTING A PATIENT. THE LIFT WOULD NOT LET UP. WAS ABLE TO LOWER, SO PT WAS LOWERED AND MOVED BACK INTO BED USING SLIDE BOARD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    703439 CIRRUS LIFT, PATIENT, NON-AC-POWERED FSA TOLLOS 600

    Patients

    Seq Age Sex Outcome Treatment
    1