BEUDAMED
    FDA Recall Terminated

    Agfa Cronex 10T Radiographic film

    Recall: Z-0471-06 · Initiated December 21, 2005

    Recall

    Recall Number
    Z-0471-06
    Event Number
    34274
    Firm
    AGFA Corp.
    FEI Number
    3001236302
    Product Code
    JAC
    Status
    Terminated
    Root Cause
    Other
    Initiated
    December 21, 2005
    Posted
    February 4, 2006
    Terminated
    April 18, 2006
    Address
    10 S Academy St, Greenville, SC, 29601-2632

    Description

    Agfa Cronex 10T Radiographic film

    Reason

    Mislabeling; Product labeled Cronex 10T actually contains Afga, Curix Ultra UVL Plus.

    Action

    Consignees were first contact by telephone followed up with a certified letter, on/about 12/21/2005.

    Distribution

    AZ, CA, CO, GA, IL, MI, NE, NV, OH, OR, WA and Canada

    Quantity

    118 boxes