{
  "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": "2026-09-17",
    "results": {
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    {
      "cfres_id": "193265",
      "product_res_number": "Z-1116-2022",
      "event_date_initiated": "2022-03-25",
      "event_date_created": "2022-05-19",
      "recall_status": "Open, Classified",
      "res_event_number": "90063",
      "product_code": "NWB",
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      "firm_fei_number": "2429304",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "city": "Center Valley",
      "state": "PA",
      "postal_code": "18034-8229",
      "additional_info_contact": "Cynthia Ow\n484-896-5000",
      "reason_for_recall": "The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.",
      "root_cause_description": "Process change control",
      "action": "On March 25, 2022, the firm contacted the affected consignee to inform them that certain manufacturing changes by a supplier led to the possibility that a part within the bending section may crack. Olympus repaired the affected URF-V2 unit free of charge.",
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      "distribution_pattern": "US Nationwide distribution in the state of AZ.",
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        "device_name": "Endoscope, Accessories, Narrow Band Spectrum",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.1500",
        "device_class": "2"
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}