{
  "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": [
    {
      "country": "United States",
      "city": "Norcross",
      "address_1": "4775 Peachtree Industrial Blvd",
      "reason_for_recall": "Incorrect patient shift directions when the Setup reference dialog is printed out when the DICOM coordinates option is enabled for reports.",
      "address_2": "Bldg 300, #300",
      "product_quantity": "38",
      "code_info": "Version 3.10.00 - 3.20.00, inclusive",
      "center_classification_date": "20120712",
      "distribution_pattern": "US Nationwide Distribution - including the states of:  CA, CT, FL, IL, IN, KY, MI, MN,  MO, NJ, NY, NC, OH, OK, OR, PA, WA, and WI",
      "state": "GA",
      "product_description": "Monaco    Product Usage:  Planning of radiation therapy",
      "report_date": "20120718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-2007-2012",
      "initial_firm_notification": "Other",
      "product_type": "Devices",
      "event_id": "62434",
      "termination_date": "20140401",
      "more_code_info": "",
      "recall_initiation_date": "20120621",
      "postal_code": "30092-3011",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}