{
  "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": "XVI can incorrectly calculate the target position of the treatment table.",
      "address_2": "Ste 50",
      "product_quantity": "380 US",
      "code_info": "XVI R4.0 to R4.2.1, R4.5.0,  R4.5.1, and R5.0.0 to R5.0.1",
      "center_classification_date": "20140616",
      "distribution_pattern": "Worldwide Distribution - USA including the states of AZ, CT, IA, OH, MD, MI, MN, NV, TX and VA., and the countries of India, Ireland, Malta, Netherlands, South Africa and UK.",
      "state": "GA",
      "product_description": "Synergy XVI    Intended for radiation therapy treatment.",
      "report_date": "20140625",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-1724-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68255",
      "termination_date": "20170717",
      "more_code_info": "",
      "recall_initiation_date": "20140423",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}