BEUDAMED
    FDA Recall Terminated

    Stryker Orthopaedics Restoration Modular Cone Body Trials Stryker Ireland Carrigtwohill Industrial Estate Carrigtwohill County Cork, Ireland. The Cone Body Trials simulate the respective Cone Body implants and mate with the stem trials to assist the surgeon in assessing the fit of the proposed Implants. The cone body trials is an assembly of the Body and 8 mm Hex Locking Bolt. The trial stem is attached to the trial Cone body via the distal thread of the Locking bolt.

    Recall: Z-2487-2012 · Initiated April 2, 2012

    Recall

    Recall Number
    Z-2487-2012
    Event Number
    62594
    Firm
    Stryker Howmedica Osteonics Corp.
    FEI Number
    3003070421
    Product Code
    LZO
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    April 2, 2012
    Posted
    September 28, 2012
    Terminated
    June 13, 2013
    Address
    325 Corporate Drive, Mahwah, NJ, 07430

    Description

    Stryker Orthopaedics Restoration Modular Cone Body Trials Stryker Ireland Carrigtwohill Industrial Estate Carrigtwohill County Cork, Ireland. The Cone Body Trials simulate the respective Cone Body implants and mate with the stem trials to assist the surgeon in assessing the fit of the proposed Implants. The cone body trials is an assembly of the Body and 8 mm Hex Locking Bolt. The trial stem is attached to the trial Cone body via the distal thread of the Locking bolt.

    Reason

    Stryker Orthopaedics has become aware of a burr, or a metal shaving, observed in the internal threaded portion of the Cone Body Trial. The typical size of the shaving observed was 1-2 mm in length and 0.037 mm squared in cross section.

    Action

    Stryker Orthopaedics sent a Urgent Product Field Action - Product Inspection Branch Acknowledgement Form on April 2, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. All inspections must be completed immediately as per the provided Product Correction Bulletin. Please document the results of your inspection on the Tracking Log, indicating conforming devices as "Not Affected" and non-conforming devices as "To be returned." If the devices listed on your tracking log have previously been returned or are otherwise not on hand, indicate the appropriate disposition following our usual process. Please assist us in meeting our regulatory obligation by faxing back the attached Product Acknowledgment Form and Tracking Log within 10 business days to 855-251-3635. Any further questions please call 201-831-5523.

    Distribution

    Nationwide distribution

    Quantity

    10, 983 units