BEUDAMED
    FDA Recall Terminated

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, Code 00214W, 20F, 3.4cm, 20cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116.

    Recall: Z-0428-2009 · Initiated September 23, 2008

    Recall

    Recall Number
    Z-0428-2009
    Event Number
    49523
    Firm
    C R Bard Inc
    FEI Number
    3006260740
    Product Code
    KNT
    Status
    Terminated
    Root Cause
    Component design/selection
    Initiated
    September 23, 2008
    Posted
    December 12, 2008
    Terminated
    November 8, 2011
    Address
    605 N 5600 W, Salt Lake City, UT, 84116-3738

    Description

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, Code 00214W, 20F, 3.4cm, 20cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116.

    Reason

    Gastrostomy device anti-reflux valve may allow leakage from the stomach.

    Action

    Customers notified by letter (Product Field Action letter) on September 23, 2008 and instructed to remove and return any affected product to Bard Access Systems, Inc (BAS). Customers were instructed in the recall letter to respond by completing and faxing the enclosed Reply Form and Inventory Reconciliation Form. For assistance, contact BAS customer service at 800-290-1689.

    Distribution

    Worldwide Distribution including US, Latin America and countries of Canada, Japan, Finland, Norway, Sweden, Austria, Belgium, Holland, Great Britain, Italy, France, Switzerland, Spain, Germany.

    Quantity

    1992 units