{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Aizuwakamatsu",
      "state": "",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97849",
      "recalling_firm": "Aizu Olympus Co., Ltd.",
      "address_1": "3 Chome 1-1",
      "address_2": "Niiderakita",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0874-2026",
      "product_description": "Olympus OER-Mini",
      "product_quantity": "6578 units",
      "reason_for_recall": "Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance  schedules and that only properly trained personnel conduct repairs and maintenance.",
      "recall_initiation_date": "20251031",
      "center_classification_date": "20251202",
      "report_date": "20251210",
      "code_info": "Model: OER-Mini; UDI: 04953170331619; Serial #: All;",
      "more_code_info": ""
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}