BEUDAMED
    FDA Recall Terminated

    1) Drainer Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-001-05, b) DRC-001-06, c) DRC-001-15, 2) Centeze Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-002-02, b) DRC-002-05, c) DRC-002-06, d) DRC-002-08,

    Recall: Z-2560-2018 · Initiated May 2, 2018

    Recall

    Recall Number
    Z-2560-2018
    Event Number
    80021
    Firm
    Galt Medical Corporation
    FEI Number
    3000718472
    Product Code
    KGZ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 2, 2018
    Terminated
    July 20, 2020
    Address
    2220 Merritt Dr, Garland, TX, 75041-6137

    Description

    1) Drainer Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-001-05, b) DRC-001-06, c) DRC-001-15, 2) Centeze Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-002-02, b) DRC-002-05, c) DRC-002-06, d) DRC-002-08,

    Reason

    The products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bacteria can activate the inflammatory process and produce fever, chills, and hypotension in a patient.

    Action

    On approximately 05/01/2018 recall letters and customer response forms were mailed to all consignees.

    Distribution

    U.S.: MN, PA, VA, CA, UT, FL, NY, GA, LA, MO, TX, MS, OH, WA, MA, IL, KY, NC, and Puerto Rico; OUS: Canada, Australia, France, Germany, Ireland, Italy, Netherlands, Poland, Slovakia, Switzerland, Belgium, United Kingdom, Korea

    Quantity

    13210