{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "KANATA",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74637",
      "recalling_firm": "BEST THERATRONICS LTD.",
      "address_1": "413 MARCH ROAD",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-2251-2016",
      "product_description": "Best Theratronics cabinet x-ray systems intended for use in the irradiation of blood and blood products (packaged in transfusion bags) to inactivate T-lymphocytes for the prevention of Graft Versus Host Disease.",
      "product_quantity": "128",
      "reason_for_recall": "It was discovered that both the new device and the predicate device failed to comply with performance standard.",
      "recall_initiation_date": "20160506",
      "center_classification_date": "20160722",
      "termination_date": "20170801",
      "report_date": "20160803",
      "code_info": "All Raycell units with serial #'s 5000 and higher."
    }
  ]
}