{
  "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": "Elkton",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83240",
      "recalling_firm": "Terumo Cardiovascular Systems Corporation",
      "address_1": "125 Blue Ball Rd",
      "address_2": "N/A",
      "postal_code": "21921-5315",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "MI  Foreign: Japan, Belgium",
      "recall_number": "Z-2102-2019",
      "product_description": "Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation)  P/N: 3CX*NX19RW",
      "product_quantity": "52units",
      "reason_for_recall": "Capiox NX19 Oxygenator may contain a non-functioning arterial thermistor component",
      "recall_initiation_date": "20190614",
      "center_classification_date": "20190730",
      "termination_date": "20200611",
      "report_date": "20190807",
      "code_info": "Lot Numbers: XAl 1, XA28, XC07"
    }
  ]
}