{
  "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": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80764",
      "recalling_firm": "Elekta, Inc.",
      "address_1": "400 Perimeter Center Ter NE Ste 50",
      "address_2": "",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AK, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, WA, WI, WV, and WY  Australia, Canada, Ireland, New Zealand, Portugal, Singapore, South Africa, Spain, Sweden, and United Kingdom",
      "recall_number": "Z-2917-2018",
      "product_description": "MOSAIQ Oncology Information System",
      "product_quantity": "185",
      "reason_for_recall": "Order Status Remains Approved When Should Indicate Complete.",
      "recall_initiation_date": "20180803",
      "center_classification_date": "20180823",
      "termination_date": "20240923",
      "report_date": "20180829",
      "code_info": "Software Build(s) 2.64 SP3 and higher",
      "more_code_info": ""
    }
  ]
}