{
  "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": [
          "BN200952"
        ],
        "brand_name": [
          "HEXTEND"
        ],
        "generic_name": [
          "HETASTARCH"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-1555"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "HETASTARCH"
        ],
        "rxcui": [
          "310757",
          "404665"
        ],
        "spl_id": [
          "25c0562d-f3f6-4ec9-bb54-1af109af8f22"
        ],
        "spl_set_id": [
          "fc79700c-6c3b-4998-8307-4dc8c81c5041"
        ],
        "package_ndc": [
          "0409-1555-64",
          "0409-1555-54"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000184175",
          "N0000009361",
          "N0000010288",
          "M0020435"
        ],
        "pharm_class_epc": [
          "Plasma Volume Expander [EPC]"
        ],
        "pharm_class_pe": [
          "Increased Intravascular Volume [PE]"
        ],
        "pharm_class_moa": [
          "Osmotic Activity [MoA]"
        ],
        "pharm_class_cs": [
          "Starch [CS]"
        ],
        "unii": [
          "875Y4127EA"
        ]
      },
      "product_type": "Drugs",
      "event_id": "63522",
      "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",
      "recall_number": "D-184-2013",
      "product_description": "HEXTEND 6% Hetastarch in Lactated Electrolyte Injection, 500 mL, Rx only , MANUFACTURED AND DISTRIBUTED BY HOSPIRA, INC., LAKE FOREST, IL 60045,  NDC 0409-1555-54",
      "product_quantity": "11,412 bags",
      "reason_for_recall": "Lack of Assurance of Sterility: There is the potential for the solution to leak from the seal of the fill tube to the bag.",
      "recall_initiation_date": "20121022",
      "center_classification_date": "20130305",
      "termination_date": "20150331",
      "report_date": "20130313",
      "code_info": "Lot # 10-199-JT Exp. 10/13"
    }
  ]
}