{
  "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": "2026-04-01",
    "results": {
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      "status": "Ongoing",
      "city": "Center Valley",
      "state": "PA",
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      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89942",
      "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",
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      "distribution_pattern": "US Nationwide distribution.",
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      "product_description": "BF-MP160F: EVIS EXERA Bronchofibervideoscope",
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      "reason_for_recall": "Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization",
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      "center_classification_date": "20220506",
      "report_date": "20220518",
      "code_info": "All serial numbers. UDI: 04953170289064"
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}