BEUDAMED
    FDA Recall Terminated

    Liko Universal Slingbar 450 (aluminum) used with the Viking L Patient Lift

    Recall: Z-0791-06 · Initiated January 9, 2006

    Recall

    Recall Number
    Z-0791-06
    Event Number
    34463
    Firm
    Liko, Inc.
    FEI Number
    3001451524
    Product Code
    FSA
    Status
    Terminated
    Root Cause
    Other
    Initiated
    January 9, 2006
    Posted
    April 26, 2006
    Terminated
    October 25, 2006
    Address
    842 Upper Union Street, Suite 4, Franklin, MA, 02038

    Description

    Liko Universal Slingbar 450 (aluminum) used with the Viking L Patient Lift

    Reason

    The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. This could cause an unsafe transfer. Patient may fall.

    Action

    Liko notified Distributors of the recall by letter on 1/9/06 via UPS and provided replacement Slingbars Version 2. Expanded Recall: On 6/20/06, Liko sent a 2nd recall letter expanding the recall to additonal serial numbers via Certified Mail.

    Distribution

    IL, MA, MO, PA, TN,

    Quantity

    38 units