{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Stockholm",
      "state": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66600",
      "recalling_firm": "RAYSEARCH LABORATORIES AB",
      "address_1": "Sveavaegen 9",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution in the states of: California, Colorado, Delaware, Florida, Maryland, Missouri, New Jersey, New York, Ohio, Pennsylvania, Tennessee, and Virginia.",
      "recall_number": "Z-0281-2014",
      "product_description": "Ray Station Radiation Therapy Treatment Planning System, Model Numbers 3.0, 3.5 and 4.0",
      "product_quantity": "195 units domestically",
      "reason_for_recall": "Ray Search Laboratories found an issue with the dose calculation for Elekta motorized wedges in Ray Station 3.0, 3.5 and 4.0.  The error presents when a wedge is used for a beam and the wedge angle differs from 60 degrees.",
      "recall_initiation_date": "20131023",
      "center_classification_date": "20131114",
      "termination_date": "20170217",
      "report_date": "20131120",
      "code_info": "Software version and build numbers 3.0.0.251, 3.5.0.16, 3.5.1.6, 4.0.0.14, 4.0.1.4.",
      "more_code_info": ""
    }
  ]
}