{
  "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": "Tokyo",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65082",
      "recalling_firm": "Canon Inc.",
      "address_1": "30-2, Shimomaruko 3-chome,",
      "address_2": "Ohta-ku",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and countries of: Australia, Japan, Korea, Singapore and United Kingdom.",
      "recall_number": "Z-1404-2013",
      "product_description": "Canon Full Auto Ref-Keratometer RK-F2, Catalog Number 6937B002AA.    Product Usage:  This device is intended to be used to measure the refractive power and the radius of corneal curvature of the human eye.",
      "product_quantity": "384 units",
      "reason_for_recall": "Canon Inc. had received 17 claims from our foreign  sales companies between October to November  2012 that measurement value of RK-F2\u0019s refractive  power (SPH value) sometimes indicated abnormal  value which occurs approximately 5% in probability.",
      "recall_initiation_date": "20121205",
      "center_classification_date": "20130525",
      "termination_date": "20130920",
      "report_date": "20130605",
      "code_info": "Catalog Number 6937B002AA.  All serial numbers from the first unit onward."
    }
  ]
}