{
  "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": "Irwindale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77575",
      "recalling_firm": "Biosense Webster, Inc.",
      "address_1": "15715 Arrow Hwy",
      "address_2": "N/A",
      "postal_code": "91706-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to the following states: CA, CO,  GA, IL, IN, MI, NM, NY,  OH, PA, TN, TX, UT, WA, WI.      Product was also distributed to the following countries: Germany, France, Austria, Sweden Italy, Belgium, Denmark, and Singapore.",
      "recall_number": "Z-0210-2018",
      "product_description": "SMARTABLATE RF System Generator",
      "product_quantity": "185 units total",
      "reason_for_recall": "Generator may inadvertently deliver RF energy if the foot pedal is placed in close proximity and oriented toward the Stereotaxis magnets.",
      "recall_initiation_date": "20170614",
      "center_classification_date": "20171207",
      "termination_date": "20210111",
      "report_date": "20171213",
      "code_info": "Product Codes M490006, M490007",
      "more_code_info": ""
    }
  ]
}