{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70625",
      "recalling_firm": "Akorn, Inc.",
      "address_1": "1925 W. Field Court, Suite 300",
      "address_2": "N/A",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-0405-2015",
      "product_description": "Fluticasone Propionate Nasal Spray, USP, 50 mcg per spray,  in amber glass bottle with net fill weight of 16 g that provides 120 actuations, Rx only, Manufactured by HI-TECH PHARMACAL CO., INC. Amityville, NY 11701 for Akorn Inc. 1925 W. Field Court, Suite 300 Lake Forest Illinois, 60045. NDC 50383-700-16.",
      "product_quantity": "44,448 bottles",
      "reason_for_recall": "Failed Stability Specifications: Out of specification for preservative, benazalkonium chloride.",
      "recall_initiation_date": "20150227",
      "center_classification_date": "20150305",
      "termination_date": "20171130",
      "report_date": "20150311",
      "code_info": "Lot #: 631639, Exp 01/2017."
    }
  ]
}