BEUDAMED
    FDA Recall Terminated

    UNO 102 Patient Lift

    Recall: Z-0277-06 · Initiated November 14, 2005

    Recall

    Recall Number
    Z-0277-06
    Event Number
    34059
    Firm
    Liko, Inc.
    FEI Number
    3001451524
    Product Code
    FSA
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 14, 2005
    Posted
    December 13, 2005
    Terminated
    February 20, 2008
    Address
    842 Upper Union Street, Suite 4, Franklin, MA, 02038

    Description

    UNO 102 Patient Lift

    Reason

    Incorrect length leg pin bolts may cause patient lift failures

    Action

    Liko Inc. initiated the recall to Distributors of the Recall on 11/14/05 via UPS. Direct customers will be notified by letter on /about 12/1/05.

    Distribution

    Nationwide

    Quantity

    663 units