{
  "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": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74668",
      "recalling_firm": "Elekta, Inc.",
      "address_1": "400 Perimeter Center Ter NE Ste 50",
      "address_2": "N/A",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  US nationwide, Antigua and Barbuda, Australia, Austria, Bahamas, Bahrain, Canada, Czech Republic, Germany, Hungary, South Africa, Spain, Sweden, Turkey, and United Kingdom",
      "recall_number": "Z-2293-2016",
      "product_description": "MOSAIQ Oncology Information System",
      "product_quantity": "383",
      "reason_for_recall": "It is possible that a change to an Order Set will not be saved in the current open Care Plan. This can result in a wrong chemo dose in the order.",
      "recall_initiation_date": "20160715",
      "center_classification_date": "20160727",
      "report_date": "20160803",
      "code_info": "Versions 2.50.05 and higher"
    }
  ]
}