BEUDAMED
    FDA Adverse Event Summary report: N

    UNO

    MDR report key: 3897125 · Received June 4, 2014

    Report

    Report Number
    1824206-2014-01715
    Date Received
    June 4, 2014
    Date of Event
    May 5, 2014
    Report Date
    May 5, 2014
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    HILL-ROM IS FILING THIS AS AN INITIAL REPORT AND ARE CONDUCTING A COMPLAINT INVESTIGATION AFTER RETURN OF PRODUCT TO MFR.

    Description of Event or Problem · 1

    IT WAS REPORTED TO HILL-ROM THAT FLAKES CAME OFF AT THE END OF THE SLING BAR HOOK AND GOT UNDER CAREGIVERS NAILS. REF MFR# 8030916-2014-00039.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    327942 UNO NON-AC POWERED PATIENT LIFT FSA LIKO AB UNO 102EE

    Patients

    Seq Age Sex Outcome Treatment
    1