{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Bella Vista",
      "state": "N/A",
      "country": "Australia",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84551",
      "recalling_firm": "ResMed Ltd.",
      "address_1": "1 Elizabeth Macarthur Dr",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: PA, MA, VA, TN, CT, IL, GA, FL, MT",
      "recall_number": "Z-0915-2020",
      "product_description": "ResMed Stellar, Non-invasive/invasive ventilators, Model: 100, 150",
      "product_quantity": "69",
      "reason_for_recall": "Combination of software and a component failure may cause audible alarms not to operate properly, the alarm buzzer not work, for ventilators that have a failed electronic component and, that are stored without AC power connected for more than 36 hours leading to full depletion of the battery and, that powers on automatically when connected to AC power without pressing the power switch.",
      "recall_initiation_date": "20191212",
      "center_classification_date": "20200206",
      "report_date": "20200212",
      "code_info": "Serial Number Range: 20160123307 to 22171057208"
    }
  ]
}