{
  "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": "Oxford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70241",
      "recalling_firm": "Villa Radiology Systems LLC",
      "address_1": "91 Willenbrock Rd Ste B1",
      "address_2": "N/A",
      "postal_code": "06478-1036",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of: AZ, AL, CA, CO, CT, DC, FL, IA, IL, IN, MI, MD, MS, MA, MO, NY, OH, PA, UT, TN and TX.",
      "recall_number": "Z-1079-2015",
      "product_description": "Juno DFR X-ray system",
      "product_quantity": "30 units distributed in the US",
      "reason_for_recall": "The system does not provide the appropriate audible signal, permanent activation, and manual override, although the system is in high-level control functionality",
      "recall_initiation_date": "20141214",
      "center_classification_date": "20150306",
      "termination_date": "20170316",
      "report_date": "20150318",
      "code_info": "P/N 709020"
    }
  ]
}