{
  "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": [
    {
      "country": "United States",
      "city": "Stamford",
      "address_1": "419 West Ave",
      "reason_for_recall": "Reports of failure of the device's power supply.",
      "address_2": "",
      "product_quantity": "2,062 devices",
      "code_info": "All serial numbers.",
      "center_classification_date": "20160503",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "CT",
      "product_description": "Smart CR Digital Computed Radiography System; Model Number: CR-IR346RU",
      "report_date": "20160511",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "recall_number": "Z-1599-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73668",
      "termination_date": "20180711",
      "more_code_info": "",
      "recall_initiation_date": "20160401",
      "postal_code": "06902-6343",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}