{
  "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": {},
      "product_type": "Drugs",
      "event_id": "75418",
      "recalling_firm": "Akorn Inc",
      "address_1": "1925 W Field Ct",
      "address_2": "",
      "postal_code": "60045-4862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-0124-2017",
      "product_description": "Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc., Lake Forest, IL 60045, NDC 17478-623-12.",
      "product_quantity": "29,972 bottles",
      "reason_for_recall": "Subpotent Drug: concentration of product is less than labeled amount.",
      "recall_initiation_date": "20161021",
      "center_classification_date": "20161102",
      "termination_date": "20190510",
      "report_date": "20161109",
      "code_info": "Lot: 041306A, Exp 04/19",
      "more_code_info": ""
    }
  ]
}