{
  "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": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84508",
      "recalling_firm": "RAYSEARCH LABORATORIES AB",
      "address_1": "Sveavagen 9",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, ID, IL, LA, MA, MD, ME, MI, MO, MS, MT, NC, NJ, NY, OH, OK, OR, PA, RI, TN, TX, UT, VA, VT, WA, and WI.",
      "recall_number": "Z-0736-2020",
      "product_description": "RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0 - Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the proposed treatment, and may be used to administer treatments after review and approval by the intended user. The system functionality can be configured based on user needs. The intended users of RayStation shall be clinically qualified radiation therapy staff trained in using the system.",
      "product_quantity": "956 Devices/Licences",
      "reason_for_recall": "Editing a static arc beam may unexpectedly set the MU of the beam to its initial default value of 200 MU.  If the bug is triggered, the dose is invalidated and needs to be recalculated before the plan can be approved or exported.",
      "recall_initiation_date": "20191118",
      "center_classification_date": "20191223",
      "termination_date": "20201110",
      "report_date": "20200101",
      "code_info": "Software Version Numbers:  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 ,  6.0.0.24 ,  6.1.0.26 ,  6.1.1.2 ,  6.2.0.7 ,  6.3.0.6 ,  7.0.0.19 ,  8.0.0.61 ,  8.0.1.10 ,   8.1.0.47 ,  8.1.1.8 , 8.1.2.5 , or  9.0.0.113",
      "more_code_info": ""
    }
  ]
}