{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Frisco",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71524",
      "recalling_firm": "Oxysure Systems, Inc.",
      "address_1": "10880 John W Elliott Dr Ste 600",
      "address_2": "N/A",
      "postal_code": "75033-3281",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide throughout the US and Chile, Trinidad, China",
      "recall_number": "Z-2253-2015",
      "product_description": "OxySure Model 615 disposable replacement cartridges, for portable oxygen generator.",
      "product_quantity": "1005 units",
      "reason_for_recall": "Flow rate of the recalled replacement cartridges does not meet the draft FDA standard of a minimum 6 LPM for a minimum of 15 minutes.",
      "recall_initiation_date": "20150612",
      "center_classification_date": "20150724",
      "termination_date": "20201019",
      "report_date": "20150805",
      "code_info": "lots 61-65"
    }
  ]
}