{
  "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": "Arvada",
      "state": "CO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85858",
      "recalling_firm": "LivaNova USA Inc.",
      "address_1": "14401 W 65th Way",
      "address_2": "N/A",
      "postal_code": "80004-3503",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to medical facilities in 5 states including: Minnesota, Kansas, Missouri, Utah and Washington.",
      "recall_number": "Z-2642-2020",
      "product_description": "LivaNova USA Sterile Disposable Connector,1/2x1/2, 20 units per case",
      "product_quantity": "140 units",
      "reason_for_recall": "Some packages of sterile disposable connectors contained a 3/8x1/4 reducer  instead of the specified 1/2x1/2 connector. No significant risk to health is expected as the issue is easily detectable and the different shape would prevent use of the connector.",
      "recall_initiation_date": "20191118",
      "center_classification_date": "20200717",
      "termination_date": "20210819",
      "report_date": "20200729",
      "code_info": "Item# EC2135S, Lot No. 1923900091",
      "more_code_info": ""
    }
  ]
}