{
  "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": "78880",
      "recalling_firm": "Philips Electronics North  America Corporation",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the countries of : France, Germany, Luxembourg and New Zealand.",
      "recall_number": "Z-0330-2018",
      "product_description": "CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system    CombiDiagnost R90 is a multi-functional general R/F system. It is suitable for all routine radiography and fluoroscopy exams, including specialist areas like angiography or pediatric work, excluding mammography",
      "product_quantity": "10",
      "reason_for_recall": "The tube adapter-plate green/yellow protective earthing (PE) wire was removed. and  spacers with different thickness were used to position pre-loc ring in respect to focal spot in specified distance.",
      "recall_initiation_date": "20171019",
      "center_classification_date": "20180110",
      "termination_date": "20180920",
      "report_date": "20180117",
      "code_info": "All CombiDiagnost R90   UDI  709030",
      "more_code_info": ""
    }
  ]
}