BEUDAMED
    FDA Enforcement Class II Terminated

    NON-STERILE SAMPLE, SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8FS, REF 044043700, 1 EA, NOT FOR CLINICAL USE

    Recall: Z-2796-2017 · Reported August 9, 2017

    Enforcement

    Recall Number
    Z-2796-2017
    Event ID
    77810
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Sorin Group USA, Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Telephone
    Report Date
    August 9, 2017
    Initiation Date
    June 29, 2017
    Classification Date
    July 29, 2017
    Termination Date
    April 12, 2021
    Address
    14401 W 65th Way, N/A, Arvada, CO, 80004-3503, United States

    Description

    NON-STERILE SAMPLE, SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8FS, REF 044043700, 1 EA, NOT FOR CLINICAL USE

    Reason

    Medtronic informed LivaNova that some of their DLP Pressure Disposable Display Sets are packaged in pouches which may have small pinholes (approximately 1mm or less in diameter). The result is a potential sterile barrier breach in the display sets. These display sets are included with LivaNova Perfusion Tube Sets (PTS) which were then distributed to customers.

    Code Info

    Lot Number 1627300090

    Distribution

    Nationwide

    Quantity

    1 unit