{
  "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": "Best",
      "state": "N/A",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83366",
      "recalling_firm": "Philips Medical Systems Nederlands",
      "address_1": "Veenpluis 4-6",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1997-2019",
      "product_description": "Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2",
      "product_quantity": "229",
      "reason_for_recall": "Philips has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with 21 CFR 1003.2(b)(1).    When performing Cine runs, the Azurion's automatic exposure control software may set technique factors that result in radiation emissions too low to obtain useful diagnostic images.",
      "recall_initiation_date": "20181130",
      "center_classification_date": "20190730",
      "termination_date": "20240327",
      "report_date": "20190807",
      "code_info": "software version R1.2"
    }
  ]
}