{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
          "BLA205747"
        ],
        "brand_name": [
          "HUMALOG"
        ],
        "generic_name": [
          "INSULIN LISPRO"
        ],
        "manufacturer_name": [
          "Eli Lilly and Company"
        ],
        "product_ndc": [
          "0002-7712",
          "0002-7510",
          "0002-7533",
          "0002-8799",
          "0002-7516",
          "0002-7714",
          "0002-8213",
          "0002-0800",
          "0002-8208"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "SUBCUTANEOUS"
        ],
        "substance_name": [
          "INSULIN LISPRO"
        ],
        "rxcui": [
          "242120",
          "865098",
          "1652239",
          "1652242",
          "1652639",
          "1652640",
          "1652644",
          "1652646",
          "1926331",
          "1926332",
          "2621571",
          "2621572"
        ],
        "spl_id": [
          "d0a38a0f-9d29-44eb-bfd1-c83cbcba1008"
        ],
        "spl_set_id": [
          "c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f"
        ],
        "package_ndc": [
          "0002-7510-01",
          "0002-7510-17",
          "0002-7510-99",
          "0002-7533-01",
          "0002-8799-01",
          "0002-8799-59",
          "0002-8799-61",
          "0002-7516-01",
          "0002-7516-59",
          "0002-7516-99",
          "0002-7714-01",
          "0002-7714-59",
          "0002-7714-61",
          "0002-8213-01",
          "0002-8213-05",
          "0002-0800-01",
          "0002-7712-01",
          "0002-7712-27",
          "0002-7712-61",
          "0002-8208-01",
          "0002-8208-27"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000004931",
          "N0000175453"
        ],
        "pharm_class_cs": [
          "Insulin [Chemical/Ingredient]"
        ],
        "pharm_class_epc": [
          "Insulin Analog [EPC]"
        ],
        "unii": [
          "059QF0KO0R",
          "GFX7QIS1II"
        ]
      },
      "product_type": "Drugs",
      "event_id": "89976",
      "recalling_firm": "Cardinal Health Inc.",
      "address_1": "7000 Cardinal Pl",
      "address_2": "N/A",
      "postal_code": "43017-1091",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NM only",
      "recall_number": "D-0882-2022",
      "product_description": "Humalog KwikPen, Insulin lispro injection, U-100, 100 units per mL, 5x3 mL Prefilled Pens per box, Marketed by Lilly USA, LLC, Indianapolis, IN 46285, Box NDC 0002-8799-59, Pen NDC 002-7516-59",
      "product_quantity": "1 box",
      "reason_for_recall": "TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.",
      "recall_initiation_date": "20220405",
      "center_classification_date": "20220519",
      "report_date": "20220525",
      "code_info": "Unknown",
      "more_code_info": ""
    }
  ]
}