{
  "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": [
          "ANDA072079"
        ],
        "brand_name": [
          "DIAZEPAM"
        ],
        "generic_name": [
          "DIAZEPAM"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-1273"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAMUSCULAR",
          "INTRAVENOUS"
        ],
        "substance_name": [
          "DIAZEPAM"
        ],
        "rxcui": [
          "1807459"
        ],
        "spl_id": [
          "88590f46-0e4c-4a4b-97de-05a1344514b7"
        ],
        "spl_set_id": [
          "41044928-dd1f-40bf-1fa6-709dff559124"
        ],
        "package_ndc": [
          "0409-1273-03",
          "0409-1273-32"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000175694",
          "M0002356"
        ],
        "pharm_class_epc": [
          "Benzodiazepine [EPC]"
        ],
        "pharm_class_cs": [
          "Benzodiazepines [CS]"
        ],
        "unii": [
          "Q3JTX2Q7TU"
        ]
      },
      "product_type": "Drugs",
      "event_id": "74399",
      "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-1359-2016",
      "product_description": "Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only,  Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32",
      "product_quantity": "373,850 tubes",
      "reason_for_recall": "Crystallization: Product contains particulate identified to be crystallized active ingredient.",
      "recall_initiation_date": "20160623",
      "center_classification_date": "20160712",
      "termination_date": "20180831",
      "report_date": "20160720",
      "code_info": "Lot #: 52610LL, Exp. 01 OCT 2016;  Lot #: 57660LL, Exp. 01 MAR 2017",
      "more_code_info": ""
    }
  ]
}