BEUDAMED
    FDA Recall Terminated

    Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug.

    Recall: Z-0011-04 · Initiated April 30, 2003

    Recall

    Recall Number
    Z-0011-04
    Event Number
    26293
    Firm
    GE Medical Systems Information Technologies
    FEI Number
    1030184
    Product Code
    MWI
    Status
    Terminated
    Root Cause
    Component design/selection
    Initiated
    April 30, 2003
    Posted
    October 15, 2003
    Terminated
    May 3, 2012
    Address
    4502 Woodland Corporate Blvd., Tampa, FL, 33614

    Description

    Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug.

    Reason

    Reports of broken plug ground pins on AC power cords for patient monitors.

    Action

    The recalling firm mailed a Recall Notification Letter with response form and corretive power cords beginning on April 30, 2003 until August 14, 2003 as corrective cords became available. Consignees were instructed on how to determine if they have the recalled cords and to destroy any found by cutting the plug from the wire. Also corrective AC power cords were provided to each consignee.

    Distribution

    The recalled AC power cords were distributed to approximately 2600 Domestic hospital accounts nationwide and 180 international accounts.

    Quantity

    16,339 Power Cords