BEUDAMED
    FDA Recall Terminated

    PERPOS PLS System, Single Use; CATALOG #'s 9045-01 & 9045-02. Interventional Spine, Inc. A sterile kit used to stabilize the spine as an aid to fusion through immobilization of the facet joints.

    Recall: Z-0045-2012 · Initiated February 3, 2011

    Recall

    Recall Number
    Z-0045-2012
    Event Number
    58461
    Firm
    Interventional Spine Inc
    FEI Number
    3003523239
    Product Code
    HXX
    Status
    Terminated
    Root Cause
    Nonconforming Material/Component
    Initiated
    February 3, 2011
    Posted
    October 13, 2011
    Terminated
    February 5, 2013
    Address
    13700 Alton Pkwy, Ste 160, Irvine, CA, 92618-1618

    Description

    PERPOS PLS System, Single Use; CATALOG #'s 9045-01 & 9045-02. Interventional Spine, Inc. A sterile kit used to stabilize the spine as an aid to fusion through immobilization of the facet joints.

    Reason

    This recall has been initiated due to drivers that may contain a burr in the distal tip preventing full seating of the driver onto the head of the facet screw, resulting in difficulty screwing the facet screw into the bone. Use of this product may result in a delay of the surgical procedure

    Action

    Interventional Spine, Inc. sent an "Urgent Recall" letter dated March 15, 2011 to all affected customers. The letter included; affected product, reason for recall and recommendations. Customers were asked to immediately examine inventory, quarantine affected product and to notify International Spine, Inc if any product remain. For information on this recall contact the firm at (949) 472-0006.

    Distribution

    Word wide Distribution: (USA) Nationwide including the states of CO, CT, FL, KY, LA, MA, NC, NY, OK, OR, TN, TX, VA, and WI; and the countries of Italy, Spain, Turkey, and the U.K.

    Quantity

    2,620 units