{
  "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": "2026-04-15",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Mississauga",
      "state": "",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80414",
      "recalling_firm": "O-Two Medical Technologies, Inc.",
      "address_1": "7575 Kimbel Street",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AK, CA, FL",
      "recall_number": "Z-2885-2018",
      "product_description": "O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System  Model#: 01EQ1000",
      "product_quantity": "3  units",
      "reason_for_recall": "Higher levels of nitrous oxide delivered than specification",
      "recall_initiation_date": "20180514",
      "center_classification_date": "20180822",
      "termination_date": "20200603",
      "report_date": "20180829",
      "code_info": "Serial Number: EQ1332-17, EQ3001-18, EQ3003-18",
      "more_code_info": ""
    }
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}