{
  "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": "Terminated",
      "city": "Stockholm",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83152",
      "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": "US Nationwide Distribution",
      "recall_number": "Z-1930-2019",
      "product_description": "RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayPlan 1 (RayStation 4.9) and RayPlan 2 (RayStation 6) .  Intended Use: software system designed for treatment planning and analysis of radiation therapy",
      "product_quantity": "744",
      "reason_for_recall": "When calculating electron Monte Carlo dose with a very large number of histories, the dose calculation may be wrong",
      "recall_initiation_date": "20171120",
      "center_classification_date": "20190703",
      "termination_date": "20230808",
      "report_date": "20190710",
      "code_info": "Software versions:   3.5.0.16 ,  3.5.1.6 ,  4.0.0.14 ,  4.0.1.4 ,  4.0.2.9 ,  4.0.3.4 ,  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 ,  4.9.0.42 ,  5.0.0.37 ,  5.0.1.11 ,  5.0.2.35 ,  5.0.3.17 ,  6.0.0.24 ,  6.1.0.26 ,  6.1.1.2  and  6.2.0.7"
    }
  ]
}