BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOLVO

    MDR report key: 3233752 · Received July 8, 2013

    Report

    Report Number
    1824206-2013-03388
    Event Type
    Malfunction
    Date Received
    July 8, 2013
    Date of Event
    March 20, 2013
    Report Date
    June 11, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COMPOSITE HOOK ON UNIVERSAL SLING BAR BROKE DURING TRANSFER OF A PT. NO INJURY ALLEGED ON THE PT. THE CAREGIVER GOT HIT IN THE FACE BY THE SLING BAR, BUT NO VISUAL INJURIES ALLEGED. REF MFR # 8030916-2013-00042.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    311697 GOLVO NON-AC POWERED PATIENT LIFT FSA LIKO AB GOLVO 7000 ES

    Patients

    Seq Age Sex Outcome Treatment
    1