{
  "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": "Ongoing",
      "city": "Maryland Heights",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83273",
      "recalling_firm": "Elekta Inc",
      "address_1": "13723 Riverport Dr Ste 100",
      "address_2": "N/A",
      "postal_code": "63043-4819",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "worldwide",
      "recall_number": "Z-2091-2019",
      "product_description": "Monaco RTP System, software versions 5.10 and 5.11, Radiation Treatment Planning System",
      "product_quantity": "1396 units",
      "reason_for_recall": "When creating 3D plans using either MU or Dose weighting modes, if the user changes the number of fractions, rescales the plan and then changes the wedge angle, the Monitor Units are scaled incorrectly.",
      "recall_initiation_date": "20190703",
      "center_classification_date": "20190727",
      "report_date": "20190807",
      "code_info": "all Monaco Radiation Treatment Planning units installed with software version 5.10 or 5.11"
    }
  ]
}