{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Barcelona",
      "state": "N/A",
      "country": "Spain",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83017",
      "recalling_firm": "Leventon S. A. U.",
      "address_1": "Calle Newton 18 24",
      "address_2": "Sant Esteve Sesrovires",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states in: AZ, CA, MA, MI, PR, and FL.",
      "recall_number": "Z-2360-2019",
      "product_description": "DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA    Provide parenteral drug infusions at a constant flow without impeding patient mobility",
      "product_quantity": "1700",
      "reason_for_recall": "The product lacks 510(k) clearance, and therefore is misbranded and must be removed from the U.S. market.",
      "recall_initiation_date": "20190523",
      "center_classification_date": "20190823",
      "termination_date": "20200608",
      "report_date": "20190904",
      "code_info": "172055L, 1721 10L, 1 807881, 181 1401  Unique Device Identifier (UDI)  08436020767470, 08436020768026"
    }
  ]
}