{
  "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": "Completed",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
          "ANDA076517"
        ],
        "brand_name": [
          "CARBOPLATIN"
        ],
        "generic_name": [
          "CARBOPLATIN"
        ],
        "manufacturer_name": [
          "Hospira, Inc."
        ],
        "product_ndc": [
          "61703-339"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "CARBOPLATIN"
        ],
        "rxcui": [
          "597195"
        ],
        "spl_id": [
          "0ddf4411-7138-412a-908a-fadf22bdfb79"
        ],
        "spl_set_id": [
          "c3ae9880-44bb-4f4e-93d8-8a5e21708a30"
        ],
        "package_ndc": [
          "61703-339-18",
          "61703-339-22",
          "61703-339-50",
          "61703-339-56"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000175413",
          "N0000175073"
        ],
        "pharm_class_epc": [
          "Platinum-based Drug [EPC]"
        ],
        "unii": [
          "BG3F62OND5"
        ]
      },
      "product_type": "Drugs",
      "event_id": "63548",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "N/A",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico.",
      "recall_number": "D-153-2013",
      "product_description": "Carboplatin Injection, 600 mg/60 mL (10 mg/mL), 60 mL, Cytotoxic Agent, Sterile, Multi-Dose Vial, Rx only, For IV Use, Hospira, Inc., Lake Forest, IL 60045, Product of Australia, NDC 61703-339-56.",
      "product_quantity": "23,315 vials",
      "reason_for_recall": "Crystallization: Product is being recalled due to visible particulates identified during a retain sample inspection. Findings have identified the particles as Carboplatin crystals.",
      "recall_initiation_date": "20121108",
      "center_classification_date": "20130206",
      "termination_date": "20170320",
      "report_date": "20130213",
      "code_info": "Lot #: Z021650AA, Exp. 08/2013",
      "more_code_info": ""
    }
  ]
}