BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNIVERSAL SLINGBAR

    MDR report key: 3233779 · Received July 11, 2013

    Report

    Report Number
    1824206-2013-03463
    Event Type
    Malfunction
    Date Received
    July 11, 2013
    Date of Event
    June 20, 2013
    Report Date
    June 28, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COMPLAINT RECORD STATES THAT THE COMPOSITE HOOK ON A UNIVERSAL SLING BAR 450 BROKE DURING TRANSFER OF A PT. NO INJURY ALLEGED. REF MFR # 8030916-2013-00048.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    320068 UNIVERSAL SLINGBAR NON-AC POWERED PATIENT LIFT FSA LIKO AB UNIV SLINGBAR 450

    Patients

    Seq Age Sex Outcome Treatment
    1