BEUDAMED
    FDA Adverse Event Death Summary report: N

    UNO

    MDR report key: 1719208 · Received June 8, 2010

    Report

    Report Number
    8030916-2010-00002
    Event Type
    Death
    Date Received
    June 8, 2010
    Date of Event
    April 27, 2010
    Report Date
    May 10, 2010
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION IS ON GOING. REQUEST HAS BEEN MADE FOR PRODUCT USED IN THE ALLEGED INCIDENT TO BE RETURNED TO THE MFR FOR ANALYSIS.

    Description of Event or Problem · 1

    FACILITY ALLEGES, THAT WHILE TRANSFERRING A PT FROM BED TO A CHAIR, THERE WAS A LOUD NOISE AND THE PT FELL TO THE FLOOR. THE NURSING HOME PT DIED TWO DAYS LATER. CAUSE OF DEATH IS UNK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNO NON-AC POWERED PATIENT LIFT FSA LIKO AB UNO 102EE

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Death