BEUDAMED
    FDA Recall Terminated

    Sabina I and II EM/EE Patient Lift

    Recall: Z-0877-05 · Initiated September 24, 2004

    Recall

    Recall Number
    Z-0877-05
    Event Number
    31193
    Firm
    Liko, Inc.
    FEI Number
    3001451524
    Product Code
    FNG
    Status
    Terminated
    Root Cause
    Other
    Initiated
    September 24, 2004
    Posted
    June 8, 2005
    Terminated
    June 20, 2007
    Address
    842 Upper Union St., Suite 4, Franklin, MA, 02038

    Description

    Sabina I and II EM/EE Patient Lift

    Reason

    Incorrect length support screws may cause patient lift failure

    Action

    Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites.

    Distribution

    Canada

    Quantity

    531 units