{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Stockholm",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81269",
      "recalling_firm": "RAYSEARCH LABORATORIES AB",
      "address_1": "Sveavagen 9",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0294-2019",
      "product_description": "RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6 and RayStation 7, a  stand-alone software treatment planning system.",
      "product_quantity": "110 units",
      "reason_for_recall": "Robust optimization for plans using beam set + background dose is not supported in RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6 and RayStation 7.",
      "recall_initiation_date": "20180921",
      "center_classification_date": "20181030",
      "termination_date": "20200616",
      "report_date": "20181107",
      "code_info": "Software, include version number:  4.5.0.19 ,  4.5.1.14 , 4.5.2.7 ,  4.7.0.15 ,  4.7.1.10,  4.7.2.5 ,  4.7.3.13 ,  4.7.4.4 ,  4.7.5.4 ,  5.0.0.37 ,  5.0.1.11 , 5.0.2.3 ,  6.0.0.24 ,  6.1.0.26 ,  6.1.1.2 ,  6.2.0.7 ,  7.0.0.19"
    }
  ]
}