BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNO 120EE

    MDR report key: 2630860 · Received May 14, 2012

    Report

    Report Number
    8030916-2012-00057
    Event Type
    Other
    Date Received
    May 14, 2012
    Date of Event
    May 16, 2012
    Report Date
    May 16, 2012
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    FACILITY COULD NOT FIND ANY FAULT ON LIFT, SLING BAR OR SLING. MANUFACTURER TOGETHER WITH AT, AT FACILITY THINKS THAT THE SLING WAS NOT CORRECTLY APPLIED TO SLING BAR AT THE TIME OF THE INCIDENT. INSTRUCTION GUIDE FOR SLING 7EN160165-04, AND LIFT 7EN150104-02 STATES THAT: "BEFORE THE PATIENT IS LIFTED FROM THE UNDERLYING SURFACE, BUT AFTER THE STRAPS HAVE BEEN FULLY EXTENDED, MAKE SURE THE STRAPS ARE PROPERLY CONNECTED TO THE SLING BAR."

    Description of Event or Problem · 1

    WHEN TRANSFERRING A PATIENT FROM WHEELCHAIR TO BED, ONE OF THE SLING LOOPS ON THE HEAD SIDE CAME LOOSE SO THAT THE PATIENT FELL TOWARDS THE FLOOR. THE STAFF WERE ABLE TO EASE THE FALL, AND THE PATIENT ENDED UP WITH A COUPLE OF ABRASIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNO 120EE NON-AC POWERED PATIENT LIFT FSA LIKO AB 2010004

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR