{
  "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": [
    {
      "country": "United States",
      "city": "Mason",
      "address_1": "7555 Innovation Way",
      "reason_for_recall": "There is a potential for a component failure of the device which could necessitate medical intervention.",
      "address_2": "",
      "product_quantity": "298",
      "code_info": "Model Numbers: PRO235, PRO240, PRO245 and PRO250    Lot Numbers: 65622 to 66773",
      "center_classification_date": "20161109",
      "distribution_pattern": "Nationwide Distribution to the follwoing states: AL, AR, AZ, CA, CT, FL, GA, IL, KS, MD, MI, MN, MO, MS, NC, NM, NY, OH, OK, PA, SC, TN, TX, VA, VT & WI.    Product was also shipped to the following countries: Poland and Switzerland",
      "state": "OH",
      "product_description": "AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip  Product is used for the occlusion of the heart's left atrial appendage, under direct visualization, in conjunction with other open cardiac surgical procedures.",
      "report_date": "20161116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AtriCure, Inc.",
      "recall_number": "Z-0377-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "75178",
      "termination_date": "20180215",
      "more_code_info": "",
      "recall_initiation_date": "20160922",
      "postal_code": "45040-9695",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}