BEUDAMED
    FDA Enforcement Class II Terminated

    Pilling Modular Verres Body/Obturator, Product Code 140880

    Recall: Z-1178-2016 · Reported March 23, 2016

    Enforcement

    Recall Number
    Z-1178-2016
    Event ID
    73267
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Teleflex Medical
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    March 23, 2016
    Initiation Date
    January 8, 2015
    Classification Date
    March 16, 2016
    Termination Date
    April 14, 2017
    Address
    2917 Weck Dr, Research Triangle Park, NC, 27709-0186, United States

    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).

    Code Info

    Lot K3

    Distribution

    US Distribution to the state of : UT

    Quantity

    8