{
  "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 III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71737",
      "recalling_firm": "Akorn, Inc.",
      "address_1": "1925 W. Field Court, Suite 300",
      "address_2": "",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1429-2015",
      "product_description": "IC-GREEN (indocyanine green for injection, USP), 25 mg Kit (NDC 17478-701-02, UPC 3 17478-701-02 6) containing 6-count IC-Green Vials 25 mg (NDC 17478-701-25, barcode (01)00317478701255) and 6-count 10 mL Sterile Aqueous Solvent Ampules (NDC 17478-701-10, UPC 3 17478-701-10 1) per carton, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL  60045.",
      "product_quantity": "370 kits",
      "reason_for_recall": "Subpotent Drug: Low out-of-specification potency result of the drug product.",
      "recall_initiation_date": "20150420",
      "center_classification_date": "20150911",
      "termination_date": "20170126",
      "report_date": "20150923",
      "code_info": "Lot #: Kit: 071374; IC-Green: 041514, Exp 10/16",
      "more_code_info": ""
    }
  ]
}