{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90063",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8229",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of AZ.",
      "recall_number": "Z-1116-2022",
      "product_description": "Olympus Uretero-reno videoscope, Model No. URF-V2",
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      "reason_for_recall": "The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.",
      "recall_initiation_date": "20220325",
      "center_classification_date": "20220519",
      "report_date": "20220525",
      "code_info": "1 unit, serial number 2825505F  UDI 04953170343582",
      "more_code_info": ""
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}