{
  "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": [
    {
      "country": "United States",
      "city": "Atlanta",
      "address_1": "400 Perimeter Center Ter Ne",
      "reason_for_recall": "Memory can become corrupted when creating a fused study via drag and drop in Leksell GammaPlan 10.2.",
      "address_2": "Ste 50",
      "product_quantity": "10",
      "code_info": "Software 10.2",
      "center_classification_date": "20150605",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including states: IL, OH, PA, TX, and WI; and countries of: Germany, Japan and United Kingdom.",
      "state": "GA",
      "product_description": "Laksell GammaPlan, a computer based dose planning system specifically designed for use with Leksell Gamma Knife, radiation therapy treatment.",
      "report_date": "20150617",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-1719-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71295",
      "termination_date": "20160112",
      "recall_initiation_date": "20150601",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}