{
  "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": "2026-03-18",
    "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": "82092",
      "recalling_firm": "Akorn Inc",
      "address_1": "1925 W Field Ct Ste 300",
      "address_2": "",
      "postal_code": "60045-4862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, including Puerto Rico.",
      "recall_number": "D-0515-2019",
      "product_description": "Clobetasol Propionate Emollient Cream 0.05%, a) 30 gram (NDC 50383-270-30) and b) 60 gram (NDC 50383-270-60) tubes, Rx only. Manufacturer: Akorn Inc. 369 Bayview Ave., Amityville, NY 117701.",
      "product_quantity": "a) 4896 tubes; b) 5064 tubes",
      "reason_for_recall": "Failed Stability Specification; out of specification (OOS) results for a preservative at 9 month stability study.",
      "recall_initiation_date": "20190125",
      "center_classification_date": "20190220",
      "termination_date": "20201103",
      "report_date": "20190227",
      "code_info": "a) 357052, exp 4/19/19  b) 356892, exp 4/16/19 and 356927, exp 4/15/19",
      "more_code_info": ""
    }
  ]
}