{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Westlake",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68982",
      "recalling_firm": "Radiometer America Inc",
      "address_1": "810 Sharon Dr",
      "address_2": "N/A",
      "postal_code": "44145-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) in the states of AZ, CA, MO, MS, TX and UT. and the countries of:  Austrialia, Austria, France, UK, Italy, Japan, Spain, India, and the Netherlands.",
      "recall_number": "Z-2597-2014",
      "product_description": "RADIANCE v. 2.4X, 2.5X and 2.6X    Product Usage:  RADIANCE is a data processing application for clinical use intended to monitor, collect, store, retrieve and process laboratory data. RADIANCE is also intended to control clinical analyzers providing laboratory data.",
      "product_quantity": "N/A",
      "reason_for_recall": "",
      "recall_initiation_date": "20140728",
      "center_classification_date": "20140905",
      "termination_date": "20141015",
      "report_date": "20140917",
      "code_info": "Verions 2.4X, 2.5X and 2.6X"
    }
  ]
}