{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Stockholm",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82662",
      "recalling_firm": "Elekta Instrument AB",
      "address_1": "Kungstensgatan 18",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide distribution to GA, MD, NJ, PA, PR, WA.    International distribution to Australia, Belgium, France, Germany, Hong Kong, Italy, Japan, Korea, Democratic People's Republic of, Netherlands, Romania, Russian Federation, Spain, Turkey, United Kingdom.",
      "recall_number": "Z-1412-2019",
      "product_description": "Leksell GammaPlan 11.1    Product Usage:  Leksell GammaPlan is a computer-based system designed for Leksell Gamma Knife treatment planning.",
      "product_quantity": "52 devices",
      "reason_for_recall": "The margin tool in Leksell GammaPlan 11.1 systematically overestimates margin in certain areas of the volume.",
      "recall_initiation_date": "20180627",
      "center_classification_date": "20190523",
      "report_date": "20190529",
      "code_info": "Software Version 11.1"
    }
  ]
}