{
  "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-2103-2019",
      "product_description": "Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280  Exported only to Japan for inclusion into convenience kits that are sold only  within the Japanese market",
      "product_quantity": "78 units",
      "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: XA28, XC12, XC25, XD05, XD27"
    }
  ]
}