{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Wayne",
      "address_1": "10 Highpoint Dr",
      "reason_for_recall": "The suction button on the ED-530XT endoscope may become lodged (stuck) in the active position following the use of x-ray contrast agents during ERCP procedures.",
      "address_2": "",
      "product_quantity": "256 units",
      "code_info": "ED-530XT - Part #202B1237697D; ED-250XT5 and ED-250XL5 - Part #202B1260196A; ED-450XT5 - Part #202B1260211A and ED-450XL5 - Part #202B1237681",
      "center_classification_date": "20150917",
      "distribution_pattern": "Distributed in the US and Canada.",
      "state": "NJ",
      "product_description": "Fujifilm Medical Endoscope for the duodenum and upper G.I. tract. ED-530XT, ED-250XT5,  ED-250XL5, ED-450XT5, and ED-450XL5 Endoscope Operation Manuals.",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "recall_number": "Z-2778-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71695",
      "termination_date": "20170525",
      "more_code_info": "",
      "recall_initiation_date": "20150630",
      "postal_code": "07470-7431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}