BEUDAMED
    FDA Recall Terminated

    Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A Teleflex Company, Manufactured for: Weck Closure Systems, 2917 Weck Drive, Research Triangle park, NC 27709, USA.

    Recall: Z-0418-05 · Initiated May 21, 2003

    Recall

    Recall Number
    Z-0418-05
    Event Number
    30639
    FEI Number
    3005747797
    Product Code
    GDO
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 21, 2003
    Posted
    January 25, 2005
    Terminated
    January 31, 2005
    Address
    1 Weck Dr., Weck, Research Triangle Park, NC, 27709

    Description

    Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A Teleflex Company, Manufactured for: Weck Closure Systems, 2917 Weck Drive, Research Triangle park, NC 27709, USA.

    Reason

    Some stylets were not bent sufficiently during the packaging process to preclude them from sliding back into the cannula during shipment.

    Action

    Consignees were notified by letter sent via Federal Express on/about 05/21/2003.

    Distribution

    Nationwide

    Quantity

    667 units