BEUDAMED
    FDA Recall Terminated

    Ross 22 FR Magna-Port Gastrostomy Tube, Item #51366.

    Recall: Z-0200-04 · Initiated November 14, 2003

    Recall

    Recall Number
    Z-0200-04
    Event Number
    27691
    Firm
    Ross Products Division, Abbott Laboratories
    FEI Number
    1000136098
    Product Code
    KNT
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 14, 2003
    Posted
    July 20, 2004
    Terminated
    October 24, 2008
    Address
    625 Cleveland Ave, Columbus, OH, 43215-1754

    Description

    Ross 22 FR Magna-Port Gastrostomy Tube, Item #51366.

    Reason

    An increase in reported balloon failures, which may result in tube displacement.

    Action

    The firm notified their customers on 11/14/2003 by telephone, fax, and FedEx. Product will be returned.

    Distribution

    Nationwide. Worldwide.