{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hamburg",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81706",
      "recalling_firm": "Philips Medical Systems Gmbh, DMC",
      "address_1": "Development And Manufacturing Ctr.",
      "address_2": "Rontgenstr. 24",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) to states of: AZ, CA, GA, IL, MN, MO, MT, NJ, OH, TX, UT & VA; and to countries of: Australia, Austria, Bangladesh, Belgium, Chile C¿te D'Ivoire, Czech Republic. Egypt, Ethiopia, France, Germany, Ghana, Iran, Italy, Jordan, Latvia, Lebanon, Luxembourg, Malaysia, Martinique, Mexico, Nepal, Netherlands, New Zealand, Philippines, Portugal  Russian Federation, Rwanda, Saudi Arabia, Serbia, South Africa, Spain, Switzerland, Turkey, United Arab Emirates and United Kingdom.",
      "recall_number": "Z-0612-2019",
      "product_description": "Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030    Stationary Fluoroscopic X-ray System",
      "product_quantity": "146",
      "reason_for_recall": "kV/mA lockin not functioning as specified which may result in the patient receiving an increased radiation dose.",
      "recall_initiation_date": "20181107",
      "center_classification_date": "20190212",
      "termination_date": "20200902",
      "report_date": "20190220",
      "code_info": "All CombiDiagnost systems with software version 1.0.0, 1.0.1 and 1.0.2"
    }
  ]
}