{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Stockholm",
      "state": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90505",
      "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 NJ and TX.",
      "recall_number": "Z-1299-2022",
      "product_description": "RayStation 11B",
      "product_quantity": "26",
      "reason_for_recall": "This notice concerns two issues found related to the display of Linear Energy Transfer (LET) in RayStation   11B including some service packs. First, when using a dose threshold for an evaluation dose, LET display  might be misleading. Second, a displayed beam-specific LET distribution can sometimes be out of sync   with the selected beam.",
      "recall_initiation_date": "20220610",
      "center_classification_date": "20220628",
      "termination_date": "20240611",
      "report_date": "20220706",
      "code_info": "UDI-DI 0735000201042620211208 Software version numbers 12.0.0.932, 12.1.0.1221, 12.0.3.68",
      "more_code_info": ""
    }
  ]
}