{
  "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": "Atlanta",
      "address_1": "400 Perimeter Center Ter Ne",
      "reason_for_recall": "Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.",
      "address_2": "Ste 50",
      "product_quantity": "45",
      "code_info": "Versions 3.10.00 and later",
      "center_classification_date": "20130925",
      "distribution_pattern": "Nationwide Distribution including AK, CA, CO, CT, FL, IL, IN, MI, MN, MO, NC, NJ, NY, OH, OK, OR, PA, SC, TN, TX, WA and Puerto Rico.",
      "state": "GA",
      "product_description": "Monaco RTP System    Radiation treatment planning",
      "report_date": "20131002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-2276-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65996",
      "termination_date": "20140508",
      "recall_initiation_date": "20130702",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}