BEUDAMED
    FDA Recall Terminated

    Siemens Mevatron Linear Accelerator Systems; Mevatron M 7440, Part No.: 5672977; Mevatron M 6700, Part No.: 5693908; Mevatron M 6730, Part No.: 5694005; Mevatron M 7140, Part No.: 5694104; Mevatron M 7400, Part No.: 5694153; Mevatron M 7445, Part No.: 5694203; Mevatron M 6300, Part No.: 8317000; Mevatron M 6740, Part No.: 8319758; Mevatron MD, Part No.: 8319808; Mevatron ME, Part No.: 8490005; Mevatron MDX, Part No.: 8496200; Mevatron M2 6300, Part No.: 9401316; Mevatron M-2 6700, Part No.: 9401407; Mevatron M2 6740, Part No.: 9401506; Mevatron MD2, Part No.: 09401654; and Mevatron MDX-2, Part No.: 9401746 Siemens Medical Solutions USA, Inc., Concord, CA

    Recall: Z-0852-2008 · Initiated July 27, 2007

    Recall

    Recall Number
    Z-0852-2008
    Event Number
    45991
    Firm
    Siemens Medical Solutions USA, Inc
    FEI Number
    2937457
    Product Code
    IYE
    Status
    Terminated
    Root Cause
    Component design/selection
    Initiated
    July 27, 2007
    Posted
    February 19, 2008
    Terminated
    April 29, 2011
    Address
    4040 Nelson Ave, Concord, CA, 94520-1200

    Description

    Siemens Mevatron Linear Accelerator Systems; Mevatron M 7440, Part No.: 5672977; Mevatron M 6700, Part No.: 5693908; Mevatron M 6730, Part No.: 5694005; Mevatron M 7140, Part No.: 5694104; Mevatron M 7400, Part No.: 5694153; Mevatron M 7445, Part No.: 5694203; Mevatron M 6300, Part No.: 8317000; Mevatron M 6740, Part No.: 8319758; Mevatron MD, Part No.: 8319808; Mevatron ME, Part No.: 8490005; Mevatron MDX, Part No.: 8496200; Mevatron M2 6300, Part No.: 9401316; Mevatron M-2 6700, Part No.: 9401407; Mevatron M2 6740, Part No.: 9401506; Mevatron MD2, Part No.: 09401654; and Mevatron MDX-2, Part No.: 9401746 Siemens Medical Solutions USA, Inc., Concord, CA

    Reason

    Door Hinge failures; loose or falling off (Stationary Structure Doors)

    Action

    Stationary Door Hinges will be replaced on each device by the recalling firm's technician visits.

    Distribution

    Worldwide- USA including the states of Missouri, Georgia, Delaware, Texas, Ohio, Alabama, Kentucky, Florida, California, North Carolina, New Jersey, New York, Illinois, Pennsylvania, Colorado, Tennessee, Arizona, Pennsylvania, Virginia, New Jersey, Michigan, Wisconsin, Indiana, Nebraska, Montana, Kansas, Mississippi, Rhode Island, Washington, South Carolina, Maryland, New Hampshire, Maine, Arkansas, Idaho, Missouri, Louisiana, Oklahoma, North Dakota, Minnesota, Massachusetts, and The District of Columbia and countries of Canada and Mexico.

    Quantity

    1,284 total for recalls Z-0850-0852-2008