{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66705",
      "recalling_firm": "Philips Medical Systems, Inc.",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including MN, NH, DE, OR, MA, TX, OH, FL, CA, WA, and SC.",
      "recall_number": "Z-0431-2014",
      "product_description": "Easy Diagnost Eleva    Universal Fluoroscopic applications",
      "product_quantity": "19 devices",
      "reason_for_recall": "The delivered application software was an outdated version to the model of equipment.",
      "recall_initiation_date": "20131030",
      "center_classification_date": "20131202",
      "termination_date": "20170109",
      "report_date": "20131211",
      "code_info": "706050, 706083, 706088"
    }
  ]
}