{
  "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": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71706",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "10 Highpoint Dr",
      "address_2": "N/A",
      "postal_code": "07470-7431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide US and Canada",
      "recall_number": "Z-2806-2015",
      "product_description": "Fujifilm Processor EPX 2500 High Definition Endoscopy; (Sales Brochure).  For use in endoscopic procedures.  Used to observe, record and capture images.",
      "product_quantity": "multiple",
      "reason_for_recall": "The EPX-2500 Operation Manual and sales brochure incorrectly identify that the ED-530XT endoscope is meant to be used with the EPX-2500 Processor.  The Operation Manual and sales brochure state that when the ED-530XT endoscope is used with the 2500 processor, a \"super image\" is displayed when it is actually a \"standard image\" that is displayed.",
      "recall_initiation_date": "20150630",
      "center_classification_date": "20150922",
      "termination_date": "20170525",
      "report_date": "20150930",
      "code_info": "2500.0312.00 and 2500.0312.01"
    }
  ]
}