{
  "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": [
          "ANDA077548"
        ],
        "brand_name": [
          "ONDANSETRON"
        ],
        "generic_name": [
          "ONDANSETRON"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-4755",
          "0409-4759"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAMUSCULAR",
          "INTRAVENOUS"
        ],
        "substance_name": [
          "ONDANSETRON HYDROCHLORIDE"
        ],
        "rxcui": [
          "283504",
          "1740467"
        ],
        "spl_id": [
          "f4d4b538-f4fd-49d7-ac02-b72d48c52e59"
        ],
        "spl_set_id": [
          "6a11f61b-2318-4382-2b91-4366e4bb53fa"
        ],
        "package_ndc": [
          "0409-4755-18",
          "0409-4755-03",
          "0409-4759-01"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "NMH84OZK2B"
        ],
        "upc": [
          "040947550329"
        ]
      },
      "product_type": "Drugs",
      "event_id": "66422",
      "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 and Puerto Rico",
      "recall_number": "D-013-2014",
      "product_description": "Ondansetron Injection, USP, 4 mg/2 mL (2 mg/mL), 2 mL Single-dose Vial, Rx Only, Sterile, Hospira Inc., Lake Forest IL 60045, USA, NDC 0409-4755-03",
      "product_quantity": "681,400 vials",
      "reason_for_recall": "Presence of Particular Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.",
      "recall_initiation_date": "20130924",
      "center_classification_date": "20131120",
      "termination_date": "20141006",
      "report_date": "20131127",
      "code_info": "29-484-DK* and 29-510-DK* Exp 05/01/2015  (lot number may be proceeded with an 01)",
      "more_code_info": ""
    }
  ]
}