{
  "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": "76905",
      "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": "US Nationwide Distribution",
      "recall_number": "Z-3128-2017",
      "product_description": "Fujifilm Endoscope   Model ED-530XT      Product Usage:  This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other purposes.",
      "product_quantity": "260 manuals in total",
      "reason_for_recall": "Fujifilm is reporting a corrective action due to an FDA inspection.",
      "recall_initiation_date": "20150309",
      "center_classification_date": "20170912",
      "termination_date": "20180702",
      "report_date": "20170920",
      "code_info": "For Manual Code 202B1259902B, 140417-3.0-DT-US2 - 157 manuals were distributed  For Manual Code 202B1237697D, 140408-5.0-DT-US2 - 103 manuals were distributed"
    }
  ]
}