{
  "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": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "NDA018667"
        ],
        "brand_name": [
          "FUROSEMIDE"
        ],
        "generic_name": [
          "FUROSEMIDE"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-6102"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAMUSCULAR",
          "INTRAVENOUS"
        ],
        "substance_name": [
          "FUROSEMIDE"
        ],
        "rxcui": [
          "1719286",
          "1719290",
          "1719291"
        ],
        "spl_id": [
          "0d4a39f2-904e-434a-9af1-83bb4febf124"
        ],
        "spl_set_id": [
          "39fd32f2-6bb7-4a65-d298-e48d26bc80c7"
        ],
        "package_ndc": [
          "0409-6102-19",
          "0409-6102-02",
          "0409-6102-18",
          "0409-6102-04",
          "0409-6102-20",
          "0409-6102-10"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000175366",
          "N0000175590"
        ],
        "pharm_class_pe": [
          "Increased Diuresis at Loop of Henle [PE]"
        ],
        "pharm_class_epc": [
          "Loop Diuretic [EPC]"
        ],
        "unii": [
          "7LXU5N7ZO5"
        ]
      },
      "product_type": "Drugs",
      "event_id": "65077",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "N/A",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-314-2013",
      "product_description": "Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA,  NDC 0409-6102-04",
      "product_quantity": "259,050 vials",
      "reason_for_recall": "Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.",
      "recall_initiation_date": "20130226",
      "center_classification_date": "20130506",
      "termination_date": "20141110",
      "report_date": "20130515",
      "code_info": "Lot 20-564-DK Exp. 02/14"
    }
  ]
}