{
  "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": "Lake Forest",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72491",
      "recalling_firm": "Event Medical LTD",
      "address_1": "60 Empire Dr",
      "address_2": "N/A",
      "postal_code": "92630-2244",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide) and Internationally to:  Algeria  Argentina  Australia  Austria  Bahrain  Bangladesh  Barbados  Belarus  Belgium  Bolivia  Canada  Chile  China  Colombia  Czech Rep  Ecuador  Egypt  England  Estonia  Finland  Germany  Ghana  Gibraltar  Greece  Guatemala  Holland  Hong Kong  Hungary  India  Indonesia  Iran  Iraq  Ireland  Israel  Italy  Japan  Jordan  Kenya  Korea  Kuwait  Laos  Latin America  Lebanon  Libya  Lithuania  Malaysia  Mexico  Morocco  Nepal  Netherlands  New Zealand  Norway  Pakistan  Palestine  Panama  Peru  Philippines  Poland  Portugal  Russia  Saudi Arabia  Serbia  Singapore  South Africa  Spain  Sri Lanka  Sudan  Switzerland  Syria  Taiwan  Thailand  Turkey  UAE  Ukraine  USA  Venezuela  Vietnam  Yemen  Zimbabwe",
      "recall_number": "Z-0230-2016",
      "product_description": "Inspiration Ventilator System, i Series and LS 12.1  LCD.   The Inspiration 7i / 5i Ventilator System is to be used by healthcare professionals in hospitals or healthcare facilities and intra-hospital transport.",
      "product_quantity": "6441 units total (251 units in US)",
      "reason_for_recall": "A component on the systems power board can fail in a manner which can cause the ventilator to shut down without alarming.",
      "recall_initiation_date": "20151013",
      "center_classification_date": "20151119",
      "termination_date": "20170622",
      "report_date": "20151125",
      "code_info": "All models manufactured prior to 2015 are affected"
    }
  ]
}