{
  "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": "Aizuwakamatsu",
      "state": "",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93335",
      "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": "Domestic distribution to FL, KY, MA, NJ, NY, and PA",
      "recall_number": "Z-0418-2024",
      "product_description": "PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE",
      "product_quantity": "24 incorrectly repaired units",
      "reason_for_recall": "Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.",
      "recall_initiation_date": "20231016",
      "center_classification_date": "20231129",
      "report_date": "20231206",
      "code_info": "UDI-DI 04953170363672 Serial Numbers 2942716, 2604497, 2502056",
      "more_code_info": ""
    }
  ]
}