{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Aliso Viejo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84727",
      "recalling_firm": "Microvention, Inc.",
      "address_1": "35 Enterprise",
      "address_2": "N/A",
      "postal_code": "92656-2601",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "All distribution was OUS.  The countries receiving affected product are:  Albania, Austria, Belarus, Belgium, Brazil, Bulgaria, China, Cyprus, Czech Republic, Denmark, Egypt, Finalnd, France, Georgia, Germany, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Latvia, Lebanon, Malta, Morocco, Netherlands, Norway, Poland, Portugal, Republic of Serbia, Romania, Russian Federation, Slovak Republic, Slovenia, South Africa, Spain, Sweden, Switzerland, Syria, Turkey, Ukraine, United Arab Emirates, and United Kingdom.",
      "recall_number": "Z-1399-2020",
      "product_description": "MicroVention Terumo Microplex 18, Platinum Embolization Coil, Cosmos 18, Sterile, Rx, REF numbers 180619CS-V, 180723CS-V, 180827CS-V, 180931CS-V, 181036CS-V, 181139CS-V, 181243CS-V, 181347CS-V, 181451CS-V, 181652CS-V, 181859CS-V,  182065CS-V, 182263CS-V, and 182468CS-V;    Product Usage: The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature.    The firm name on the label is MicroVention, Inc., Tustin, CA.",
      "product_quantity": "403 units",
      "reason_for_recall": "The devices may be missing the implant coil.",
      "recall_initiation_date": "20191122",
      "center_classification_date": "20200227",
      "termination_date": "20220126",
      "report_date": "20200304",
      "code_info": "Catalog/lot numbers:    180619CS-V - 1903065W1, 1904015P1, 1904225W1, 1904295W1, 1905085P1, 1905085W1, 1905175W1, and 1905205W1;    180723CS-V - 1903085W1, 1903185W1, 1904015P1, 1904175P1, 1904295W1, 1905085W1, and 1905175W1;      180827CS-V - 1903205W1, 1904015P1, 1905155W1, and 1905205W1;    180931CS-V - 1904225R1, 1903205W1, 1905175W1, and 1905225W1;    181036CS-V - 1904035R1, 1903085W1, 1903185W1, 1904225W1, 1904265W1, 1905035W1, 1905065W1, 1905175W1, and 1905205W1;    181139CS-V - 1903015L1, 1903015W1, 1903085P1, 1903085W1, 1903185W1, 1904015P1, 1904245P1, and 1904245W1;    181243CS-V - 1903015L1, 1903015W1, 1903065W1, 1903185W1, 1904015P1, 1904175P1, 1904225W1, 1904265W1, 1904295W1, 1905155W1, 1905175W1, and 1905225W1;    181347CS-V - 1903085V1, 1903135R1, 1904035R1, 1903015W1, 1903085W1, 1903205P1, 1903205W1, and 1904225W1;    181451CS-V - 1903085W1, 1903225W1, 1904015P1, 1904175P1, 1904225W1, 1904295W1, 1905105W1, and 1905135W1;    181652CS-V - 1905135R1, 1903015W1, 1903045W1, 1903085W1, 1903205W1, 1903225W1, 1904105W1, 1905105W1, and 1905225W1;    181859CS-V - 1903155P1, 1903155W1, 1903185H1, and 1905105W1;    182065CS-V - 1903045L1, 1904085Q1, 1903155W1, 1903185H1, and 1903205H1;    182263CS-V - 1904035R1; and     182468CS-V - 1903015L1, 1903135R1, 1904055R1, 1905205R1, 1904295H1, 1905025G1, 1905025H1, 1905105H1, 1905105W1, 1905135H1, and 1905205H1."
    }
  ]
}