{
  "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,
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  "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-3129-2017",
      "product_description": "Fujifilm Endoscope   Models     ED-250XL5  ED-250XT5  ED-450XT5  ED-450XL5    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 conducting a corrective action due to an FDA inspection.",
      "recall_initiation_date": "20150309",
      "center_classification_date": "20170912",
      "termination_date": "20180702",
      "report_date": "20170920",
      "code_info": "will be entered."
    }
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}