{
  "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": "78730",
      "recalling_firm": "Akorn Inc",
      "address_1": "1925 W Field Ct Ste 300",
      "address_2": "N/A",
      "postal_code": "60045-4862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0211-2018",
      "product_description": "Gabapentin Oral Solution, 250 mg/5 mL (50 mg/mL) in a 470 mL amber-colored bottle, Rx Only.  Manufactured by: Hi-Tech Pharmacal Co., Inc.  Amityville, NY 11701.  NDC:  50383-311-47",
      "product_quantity": "4,885 bottles",
      "reason_for_recall": "CGMP Deviations: Inadvertent release of a drug product with unapproved active ingredient manufacturer.",
      "recall_initiation_date": "20171215",
      "center_classification_date": "20180108",
      "termination_date": "20190410",
      "report_date": "20180117",
      "code_info": "Batch# 359774; Exp. 09/02/19",
      "more_code_info": ""
    }
  ]
}