{
  "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": [
    {
      "country": "United States",
      "city": "Wayne",
      "address_1": "10 Highpoint Dr",
      "reason_for_recall": "Fujifilm is recalling multiple endoscopes after a retrospective review.",
      "address_2": "",
      "product_quantity": "4 units",
      "code_info": "1U881A131  1U88A1A145  3U881A005",
      "center_classification_date": "20170710",
      "distribution_pattern": "US Distribution to : AL, HI and MO",
      "state": "NJ",
      "product_description": "Ultrasonic Endoscope  Model Number EG-530UT    A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripheral organs",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "recall_number": "Z-2706-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76899",
      "termination_date": "20181003",
      "more_code_info": "",
      "recall_initiation_date": "20170217",
      "postal_code": "07470-7431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}