{
  "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": "Center Valley",
      "address_1": "3500 Corporate Pkwy",
      "reason_for_recall": "Olympus has received complaints regarding the breakage of the endoscope's insertion tube bending section during surgical procedures.  Some of these complaints are associated with tissue trauma, including perforation, and insertion tubes which were stuck inside the patient and had to be surgically removed.",
      "address_2": "PO Box 610",
      "product_quantity": "1,627 units (769 URF-V2 and 858 URF-V2R)",
      "code_info": "All serial numbers",
      "center_classification_date": "20170224",
      "distribution_pattern": "Worldwide distribution-US Nationwide and country of: Canada.",
      "state": "PA",
      "product_description": "Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories    The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.",
      "report_date": "20170308",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus Corporation of the Americas",
      "recall_number": "Z-1252-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75993",
      "termination_date": "20180227",
      "more_code_info": "",
      "recall_initiation_date": "20161212",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}