{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98288",
      "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": "Letter",
      "distribution_pattern": "US Nationwide Distribution.",
      "recall_number": "Z-1452-2026",
      "product_description": "Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.",
      "product_quantity": "1 unit",
      "reason_for_recall": "Complaints of the ceramic tip of the resection sheath breaking have been received.",
      "recall_initiation_date": "20251111",
      "center_classification_date": "20260220",
      "report_date": "20260304",
      "code_info": "Model No. A2666; UDI: 04042761004244; All Lots"
    }
  ]
}