{
  "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": "73469",
      "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 Distribution.",
      "recall_number": "Z-1860-2016",
      "product_description": "Endoscope; ED-530XT Operation Manual  'Operation and Preparation' and 'Cleaning, Disinfection and Storage'",
      "product_quantity": "1473 units",
      "reason_for_recall": "This correction is in response to publicized reports of multi-drug resistant bacteria on endoscopes used for Endoscopic Retrograde Cholangiopancreatogram (ERCP) procedures.",
      "recall_initiation_date": "20151223",
      "center_classification_date": "20160531",
      "termination_date": "20180118",
      "report_date": "20160608",
      "code_info": "All  distribution dates :3/2003-4/2016"
    }
  ]
}