{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
          "NDA019445"
        ],
        "brand_name": [
          "DEXTROSE"
        ],
        "generic_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-1775"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "rxcui": [
          "727518"
        ],
        "spl_id": [
          "281f40ec-c783-4ef3-875a-48db80a082af"
        ],
        "spl_set_id": [
          "672264e3-9709-4bba-2a9d-12bf70c7396a"
        ],
        "package_ndc": [
          "0409-1775-40",
          "0409-1775-10"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "LX22YL083G"
        ]
      },
      "product_type": "Drugs",
      "event_id": "77111",
      "recalling_firm": "Hospira Inc.",
      "address_1": "600 N Field Dr",
      "address_2": "",
      "postal_code": "60045-4835",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide in the USA and Puerto Rico",
      "recall_number": "D-0862-2017",
      "product_description": "Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10",
      "product_quantity": "71,550 syringes",
      "reason_for_recall": "Presence of Particulate Matter: human hair found within an internal sample syringe.",
      "recall_initiation_date": "20170421",
      "center_classification_date": "20170524",
      "report_date": "20170531",
      "code_info": "Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02",
      "more_code_info": ""
    }
  ]
}