{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "1925 W Field Ct Ste 300",
      "reason_for_recall": "Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point",
      "address_2": "",
      "product_quantity": "4,045 units",
      "code_info": "Lot#: 1967800, Exp10/2016",
      "center_classification_date": "20160824",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only,  Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.",
      "report_date": "20160831",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Akorn, Inc.",
      "recall_number": "D-1469-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "74794",
      "termination_date": "20170721",
      "more_code_info": "",
      "recall_initiation_date": "20160727",
      "postal_code": "60045-4862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}