BEUDAMED
    FDA Recall Terminated

    Pilling Modular Verres Body/Obturator, Product Code 140880

    Recall: Z-1178-2016 · Initiated January 8, 2015

    Recall

    Recall Number
    Z-1178-2016
    Event Number
    73267
    Firm
    Teleflex Medical
    FEI Number
    3005747797
    Product Code
    GDM
    Status
    Terminated
    Root Cause
    Packaging process control
    Initiated
    January 8, 2015
    Posted
    March 16, 2016
    Terminated
    April 14, 2017
    Address
    2917 Weck Dr, Research Triangle Park, NC, 27709-0186

    Description

    Pilling Modular Verres Body/Obturator, Product Code 140880

    Reason

    Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).

    Action

    Teleflex sent an Medical Device Advisory Notification letter dated January 8, 2016, to all affected customers notifying them of the packaging error. Our records indicate that you have received products that are subject to this notification. Teleflex Medical is committed to providing high quality, safe and effective products. We sincerely apologize for any inconvenience this action may cause your operations. If you have any other questions, feel free to contact your local sales representative or Customer Service at [email protected] or 1-866-246-6990.

    Distribution

    US Distribution to the state of : UT

    Quantity

    8