{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82177",
      "recalling_firm": "Akorn Inc",
      "address_1": "1925 W Field Ct Ste 300",
      "address_2": "",
      "postal_code": "60045-4862",
      "voluntary_mandated": "",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-0511-2019",
      "product_description": "Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co, 200 Wilmont Rd Deerfield IL 60015 NDC 00363-9651-01.",
      "product_quantity": "78120 dropper bottles",
      "reason_for_recall": "Failed Stability Specification: out of specification results for Sodium Perborate",
      "recall_initiation_date": "20190204",
      "center_classification_date": "20190219",
      "termination_date": "20220729",
      "report_date": "20190227",
      "code_info": "Lot # 8D31A, Exp: 03/20;  7H98A, Exp: 07/19; 7L80A, Exp: 10/19.",
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    }
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}