{
  "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": "72351",
      "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-0295-2016",
      "product_description": "Hydrocortisone and Acetic Acid Otic Solution, USP, containing hydrocortisone (1%) and acetic acid (2%), 10 mL bottles, Rx Only, Hi-Tech Pharmacal, Amityville, NY 11701, Made in USA, NDC # 50383-901-10",
      "product_quantity": "13,896 bottles",
      "reason_for_recall": "Defective Container: Product missing safety seal around the neck of the bottle.  The product label indicates, \"Tamper Evident: Do not use if printed seal around cap is broken or missing.\"  Because the product is missing the approved component and is not consistent with the labeling, the lot is being recalled.",
      "recall_initiation_date": "20150821",
      "center_classification_date": "20151116",
      "termination_date": "20171129",
      "report_date": "20151125",
      "code_info": "Lot # 346191, Exp. 12/2016"
    }
  ]
}