BEUDAMED
    FDA Enforcement Class II Terminated

    Plastic Kit, part number CMP1084(C

    Recall: Z-1360-2017 · Reported March 8, 2017

    Enforcement

    Recall Number
    Z-1360-2017
    Event ID
    76280
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Windstone Medical Packaging, Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
    Report Date
    March 8, 2017
    Initiation Date
    January 11, 2017
    Classification Date
    February 28, 2017
    Termination Date
    May 3, 2017
    Address
    1602 4th Ave N, N/A, Billings, MT, 59101-1521, United States

    Description

    Plastic Kit, part number CMP1084(C

    Reason

    The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

    Code Info

    Lot number and expiration date 86626, 9/3/2017 87202, 9/16/2017 87481, 9/9/2017 87924, 9/17/2017 88217, 10/31/2017 88819, 10/27/2017 89271, 10/11/2017 89539, 12/7/2017 95831, 1/9/2018 96460, 4/12/2018 98055, 6/30/2018 98962, 6/22/2018 99088, 9/15/2018

    Distribution

    Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.

    Quantity

    580 kits