{
  "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": "Stockholm",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74750",
      "recalling_firm": "RAYSEARCH LABORATORIES AB",
      "address_1": "Sveavaegen 9",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AZ, CA, FL, MT, NC NY, TX, OH & WA",
      "recall_number": "Z-0079-2017",
      "product_description": "Radiation Therapy Treatment Planning System, Model 5.0",
      "product_quantity": "491 units (187 domestically & 304 internationally)",
      "reason_for_recall": "For a treatment plan consisting of multiple beam sets, the table for ROI plan dose statistics in the report may show the statistics for a beam set dose.  The error can only be triggered when using a report template where statistics for a beam set dose is included as the last dose statistics prior to the plan dose statistics.",
      "recall_initiation_date": "20160530",
      "center_classification_date": "20161013",
      "termination_date": "20170922",
      "report_date": "20161019",
      "code_info": "5.0.0.37, 5.0.1.11 and 5.0.2.35"
    }
  ]
}