BEUDAMED
    FDA Recall Terminated

    Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue approximation.

    Recall: Z-1555-2014 · Initiated March 11, 2014

    Recall

    Recall Number
    Z-1555-2014
    Event Number
    67711
    Firm
    Teleflex Medical
    FEI Number
    3005747797
    Product Code
    GAR
    Status
    Terminated
    Root Cause
    Employee error
    Initiated
    March 11, 2014
    Posted
    May 7, 2014
    Terminated
    August 14, 2017
    Address
    4024 Stirrup Creek Dr, Durham, NC, 27703-9000

    Description

    Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue approximation.

    Reason

    Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.

    Action

    Urgent Medical Device Recall Notification letters were issued on March 11, 2014 to consignees. The letter requested that customers discontinue use and quarantine any product on hand. The attached Recall Acknowledgment Form should be completed and returned to Teleflex regardless of whether affected product is on hand or not. Once received a customer service representative will contact customers with instructions on how to return the affected product. Questions should be directed to Customer Service at 1-866-246-6990.

    Distribution

    Worldwide Distribution -- USA, including the states of AL, CA, FL, GA, IL, IN, KS, LA, ME, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, PA, RI, SC, TN, TX, UT, VA, WV, and WI; and countries of Canada, Germany, and Ireland.

    Quantity

    32,271 ea.