BEUDAMED
    FDA Recall Terminated

    Universal SlingBar 600 with Quick-release Hook Product Number: 3156086 Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts

    Recall: Z-2320-2008 · Initiated July 1, 2008

    Recall

    Recall Number
    Z-2320-2008
    Event Number
    48747
    Firm
    Liko AB Alvik
    FEI Number
    6884
    Product Code
    FSA
    Status
    Terminated
    Root Cause
    Component design/selection
    Initiated
    July 1, 2008
    Posted
    September 20, 2008
    Terminated
    July 17, 2015
    Address
    7555 Lulea Sweden

    Description

    Universal SlingBar 600 with Quick-release Hook Product Number: 3156086 Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts

    Reason

    A component securing the Universal SlingBar to the patient lift, may experience a nut unthreading resulting in the sling bar detaching from the lift causing the patient to fall.

    Action

    Liko North America ,the US Distributor, notified accounts by letter dated June 30, 2008 and provided a Field Safety Notice with Safety Inspection Procedures to performed on the lift prior to use. Replacement slingbars are being provided. If you have questions, contact the Liko product distributor in your country. Contact information can be found at www.liko.com/int/distributors.asp.

    Distribution

    Nationwide