{
  "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 I",
      "openfda": {
        "application_number": [
          "ANDA074086"
        ],
        "brand_name": [
          "DOBUTAMINE"
        ],
        "generic_name": [
          "DOBUTAMINE"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "0409-2344"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "DOBUTAMINE HYDROCHLORIDE"
        ],
        "rxcui": [
          "1812168"
        ],
        "spl_id": [
          "e71e9520-871b-479d-9652-1857fceca863"
        ],
        "spl_set_id": [
          "dc537761-d5f4-488d-24ab-b2bcd2b17b7a"
        ],
        "package_ndc": [
          "0409-2344-01",
          "0409-2344-62",
          "0409-2344-02"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "0WR771DJXV"
        ]
      },
      "product_type": "Drugs",
      "event_id": "67354",
      "recalling_firm": "Hospira Inc.",
      "address_1": "375 N Field Dr",
      "address_2": "",
      "postal_code": "60045-2513",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico.",
      "recall_number": "D-1540-2014",
      "product_description": "DOBUTamine Injection, USP, 250 mg per 20 mL, 20 mL Single-dose Fliptop Vial, Rx only, Manufactured for Hospira Inc., Lake Forest, IL 60045 USA.  NDC 0409-2344-02",
      "product_quantity": "123,900 vials",
      "reason_for_recall": "Presence of Particulate Matter: Discolored solution due to a chip in the glass at the neck of the vial, also glass particulate was found within the solution.",
      "recall_initiation_date": "20140110",
      "center_classification_date": "20140818",
      "termination_date": "20150714",
      "report_date": "20140827",
      "code_info": "Lot # 27-352-DK; Exp 03/15",
      "more_code_info": ""
    }
  ]
}