{
  "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 II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "76732",
      "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-0661-2017",
      "product_description": "LATANOPROST OPHTHALMIC SOLUTION, 0.005%,  125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only,  Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12",
      "product_quantity": "107,940 bottles",
      "reason_for_recall": "Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.",
      "recall_initiation_date": "20170317",
      "center_classification_date": "20170411",
      "termination_date": "20190709",
      "report_date": "20170419",
      "code_info": "Lot # LAB15G52, LAB11G52, Exp 6/17; LAB18I52, Exp 8/17; LAB9L52, 11/17; LAB1A62, LAB9A62, Exp 12/17",
      "more_code_info": ""
    }
  ]
}