BEUDAMED
    FDA Enforcement Class II Terminated

    Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments

    Recall: Z-1867-2016 · Reported June 8, 2016

    Enforcement

    Recall Number
    Z-1867-2016
    Event ID
    73684
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Integra LifeSciences Corp.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    June 8, 2016
    Initiation Date
    March 7, 2016
    Classification Date
    May 31, 2016
    Termination Date
    March 31, 2017
    Address
    311 Enterprise Dr, N/A, Plainsboro, NJ, 08536-3344, United States

    Description

    Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments

    Reason

    Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.

    Code Info

    Catalogue No: CEV669E. All batch numbers distributed from January 2011 to February 17, 2016.

    Distribution

    AR, CA, CO, FL, IN, KY, MA, MI, NC, NJ, NY, NM, OH, TN, TX, WA and WI

    Quantity

    2,487 Instruments