BEUDAMED
    FDA Enforcement Class II Terminated

    Bausch + Lomb Stellaris Elite 23 GA Vit Cutter, Model BL5627, 7500 cpm, packaged in sterile pouches, 6/shipper.

    Recall: Z-3268-2018 · Reported October 3, 2018

    Enforcement

    Recall Number
    Z-3268-2018
    Event ID
    80837
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Bausch & Lomb Inc
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    October 3, 2018
    Initiation Date
    August 8, 2018
    Classification Date
    September 27, 2018
    Termination Date
    August 28, 2019
    Address
    3365 Tree Court Industrial Blvd, Saint Louis, MO, 63122-6615, United States

    Description

    Bausch + Lomb Stellaris Elite 23 GA Vit Cutter, Model BL5627, 7500 cpm, packaged in sterile pouches, 6/shipper.

    Reason

    The back cap separates from the body of the vitrectomy cutter.

    Code Info

    Lot numbers V9300, exp. 10/17/2018; V9807, exp. 1/7/2019; W0019, exp. 2/5/2019; and W1468, exp. 8/26/2019, UDI 00757770058907.

    Distribution

    Distribution was made to AL, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, MA, ME, MO, MT, NC, NJ, NY, OH, OK, OR, PA, TN, TX, UT, and WV. There was government distribution but no military distribution. Foreign distribution was made to Russia, Romania, Poland, The Netherlands, Jordan, Italy, Israel, Switzerland, Hungary, Greece, Guadeloupe, Great Britain, France, Spain, Singapore, Malaysia, and Thailand.

    Quantity

    103.33 cases