BEUDAMED
    FDA Recall Terminated

    Toshiba Digital Radiography System Model DFP8000D

    Recall: Z-0532-06 · Initiated November 15, 2005

    Recall

    Recall Number
    Z-0532-06
    Event Number
    34102
    Firm
    Toshiba American Med Sys Inc
    FEI Number
    2020563
    Product Code
    JAA
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 15, 2005
    Posted
    February 23, 2006
    Terminated
    July 12, 2007
    Address
    2441 Michelle Dr, Tustin, CA, 92781

    Description

    Toshiba Digital Radiography System Model DFP8000D

    Reason

    In certain conditions the FOV of the lateral plane does not coincide with the X-ray exposed area, and consequently a part of the X-ray field may not be displayed in the magnification mode.

    Action

    An Advisory Letter will be sent to customers via certified mail. Corrected software will be provided at no charge. Customers can contact their local Toshiba Service person to schedule the software update.

    Distribution

    CO, MI, & TX

    Quantity

    3