{
  "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": "62828",
      "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": "Telephone",
      "distribution_pattern": "Nationwide Distribution (USA)",
      "recall_number": "Z-2265-2012",
      "product_description": "Canon Solid State X-ray Imager (Flat Panel/Digital Imager), Digital Radiography, Models CXDI-55C, CXDI-55G and CXDI-70C. These devices are intended to replace radiographic film/screen systems in all general purpose diagnostic procedures.",
      "product_quantity": "468 units",
      "reason_for_recall": "Screws holding the 55REF circuit board are loosening and roaming inside of the sealed sensor.",
      "recall_initiation_date": "20101101",
      "center_classification_date": "20120824",
      "termination_date": "20140107",
      "report_date": "20120905",
      "code_info": "Catalog numbers 3930B002AA, 3928B002AA, and 4066B002AA."
    }
  ]
}