{
  "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": "Mason",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75373",
      "recalling_firm": "AtriCure, Inc.",
      "address_1": "7555 Innovation Way",
      "address_2": "N/A",
      "postal_code": "45040-9695",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution -- USA, in the following states AL, AR, AZ, CA, CO, CT, GA, FL, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, WA, WI, & VA; and, to the countries of Albania, Australia, Belgium, France,  Germany, Ireland, Italy, Norway, Netherlands, Poland, Sweden, Turkey, United Arab Emirates, & United Kingdom.",
      "recall_number": "Z-0653-2017",
      "product_description": "COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System.  Model Numbers: 700-001, 700-001S, 700-001MI, 700-002, and 700-003.    Intended to ablate cardiac tissue during cardiac surgery using radiofrequency (RF) energy when connected directly to the Estech Electrosurgical unit (ESU).",
      "product_quantity": "5,263",
      "reason_for_recall": "Due to product design and process control, part of the device can separate and remain behind when the device is removed that can potentially cause permanent impairment or damage to body function or structure.",
      "recall_initiation_date": "20160922",
      "center_classification_date": "20161122",
      "termination_date": "20180208",
      "report_date": "20161130",
      "code_info": "Specifically all lots manufactured prior to February 2016.  This information can be identified as the symbol for \"date of manufacture\" on the product label as: MM-YYYY, e.g. 02-2016 or earlier."
    }
  ]
}