{
  "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": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73023",
      "recalling_firm": "Philips Medical Systems",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: Nationwide Distribution in the states of FL, OH, and MO.",
      "recall_number": "Z-0745-2016",
      "product_description": "DS/US Proton Feature with Pinnacle3  Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621",
      "product_quantity": "3",
      "reason_for_recall": "In DS/US proton planning, there is a correction factor used internally to the dose engine that is calculating improperly in some cases. This can result in an incorrect dose calculation.",
      "recall_initiation_date": "20160108",
      "center_classification_date": "20160202",
      "termination_date": "20161005",
      "report_date": "20160210",
      "code_info": "Software Version 10.0.0 and 14.0.0",
      "more_code_info": ""
    }
  ]
}