{
  "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": "2026-03-18",
    "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": "92633",
      "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": "Nationwide",
      "recall_number": "Z-2344-2023",
      "product_description": "Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accessories.",
      "product_quantity": "1063 units",
      "reason_for_recall": "Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the LF-V and LF-P are no longer compatible endoscopes for reprocessing in the OERs.  The addendum highlights the following changes:  1. Removal of LF-V and LF-P as compatible with the OER  2. Change conditions for ETO gas sterilization from 12% EtO to 100% EtO  3. Removing the reusable cleaning brush for the manual cleaning. Single Use brushes  remain compatible",
      "recall_initiation_date": "20230526",
      "center_classification_date": "20230804",
      "report_date": "20230816",
      "code_info": "UDI-DI: 04953170404047 Serial Numbers: 2201375 and the last 4 digits less than 1375"
    }
  ]
}