{
  "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 I",
      "openfda": {
        "application_number": [
          "NDA018916"
        ],
        "brand_name": [
          "HEPARIN SODIUM"
        ],
        "generic_name": [
          "HEPARIN SODIUM"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-1005",
          "0409-7620",
          "0409-2222"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "HEPARIN SODIUM"
        ],
        "rxcui": [
          "1658690",
          "1658692"
        ],
        "spl_id": [
          "09688337-d13d-49c5-9235-a719ff77e8c9"
        ],
        "spl_set_id": [
          "32e34077-aff1-4ec7-f9b0-b8e240768fb8"
        ],
        "package_ndc": [
          "0409-7620-13",
          "0409-7620-03",
          "0409-7620-49",
          "0409-7620-59",
          "0409-1005-01",
          "0409-1005-20",
          "0409-2222-01",
          "0409-2222-12"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "ZZ45AB24CA"
        ]
      },
      "product_type": "Drugs",
      "event_id": "69214",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0324-2015",
      "product_description": "HEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL flexible container unit, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7620-03",
      "product_quantity": "63,378 flexible container units",
      "reason_for_recall": "Presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.",
      "recall_initiation_date": "20140911",
      "center_classification_date": "20141223",
      "termination_date": "20160104",
      "report_date": "20141231",
      "code_info": "Lot #: 41-046-JT, Exp 11/01/2015",
      "more_code_info": ""
    }
  ]
}