{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Foster City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97184",
      "recalling_firm": "Capnia Inc",
      "address_1": "1101 Chess Dr",
      "address_2": "",
      "postal_code": "94404-1102",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of PA, UT, TX, FL, MA, IA.",
      "recall_number": "Z-2198-2025",
      "product_description": "Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide Monitor",
      "product_quantity": "2160",
      "reason_for_recall": "Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO) monitor may have residual carbon monoxide and volatile organic compounds present due to insufficient aeration of the cannula's carbon filter prior to sealing, which may lead to higher than expected ETOCc scores during clinical evaluations.",
      "recall_initiation_date": "20250421",
      "center_classification_date": "20250729",
      "report_date": "20250806",
      "code_info": "Monitor UDI-DI: 00858481006017. Lot (C20206): 231220",
      "more_code_info": ""
    }
  ]
}