BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNO

    MDR report key: 1150084 · Received August 29, 2008

    Report

    Report Number
    3006252983-2008-00028
    Event Type
    Other
    Date Received
    August 29, 2008
    Report Date
    July 30, 2008
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    FACILITY REPORTS THAT WHILE USING AN UNO PT LIFT WITH A NON-LIKO MFG SLING THAT THE LOOP OF THE SLING CAME OFF AND THE RESIDENT FELL/TUMBLED TO THE FLOOR. RESIDENT SUFFERED MINOR LACERATION TO THE EAR AS HER HEAD HIT THE BED. FACILITY ATTRIBUTES INCIDENT TO USE OF NON-LIKO MFG SLING IN USE AT THE TIME OF THE REPORTED INCIDENT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Other