{
  "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": "Terminated",
      "city": "Mettawa",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82393",
      "recalling_firm": "Vyaire Medical",
      "address_1": "26125 N Riverwoods Blvd",
      "address_2": "N/A",
      "postal_code": "60045-3420",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution.  US nationwide, Brazil, Canada, Chile, Colombia, Ecuador, Hong Kong, Hungary, Israel, India, Jordan, Korea, Kuwait, Kazakhstan, Lebanon, Macedonia, Mexico, Malaysia , Myanmar, Netherlands, New Zealand, Oman, Peru, Qatar, Russian Federation, Saudi Arabia, Thailand, Turkey, United Republic of Tanzania, South Africa, Panama, and Viet Nam.",
      "recall_number": "Z-1386-2019",
      "product_description": "enFlow Disposable Cartridge with IV Extension Set, used for intravenous warming therapy with fluid and blood solutions.",
      "product_quantity": "5,782,820 units total",
      "reason_for_recall": "Testing has demonstrated aluminum elution  from the enFlow Disposable Cartridge during fluid warming.",
      "recall_initiation_date": "20190313",
      "center_classification_date": "20190626",
      "termination_date": "20200922",
      "report_date": "20190703",
      "code_info": "Part Number: 980202EU.  All units distributed through March 7, 2019."
    }
  ]
}