BEUDAMED
    FDA Recall Terminated

    Caspar Titanium Aneurysm Clip Appliers, Catalog No/Part #: FT420T, Casper Applier F/Mini Ti-Clipsstr 146 mm, Aesculap, Inc., Center Valley, PA. 18034

    Recall: Z-0708-2008 · Initiated November 1, 2007

    Recall

    Recall Number
    Z-0708-2008
    Event Number
    46142
    Firm
    Aesculap Inc
    FEI Number
    2916714
    Product Code
    HCI
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    November 1, 2007
    Posted
    January 29, 2008
    Terminated
    March 28, 2008
    Address
    3773 Corporate Pkwy, Center Valley, PA, 18034-8217

    Description

    Caspar Titanium Aneurysm Clip Appliers, Catalog No/Part #: FT420T, Casper Applier F/Mini Ti-Clipsstr 146 mm, Aesculap, Inc., Center Valley, PA. 18034

    Reason

    Breakage: the inner rod of the applier may corrode and break

    Action

    The recalling firm issued an Import Recall Notice, on or about December 18, 2007, to all their customers to inform them of the problem and the need to return the devices .

    Distribution

    Worldwide- USA hospitals in AZ, CA, CO, IL, KY, MI, MS, ND, NM, NY, OH, OK, PA, TX, VA, WA, and WI, to sales representatives in NC, OK, and MO and shipped to distributors in CA and Canada.

    Quantity

    60 clips