{
  "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": "2026-07-29",
    "results": {
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      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        "brand_name": [
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        "substance_name": [
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        "rxcui": [
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        "is_original_packager": [
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        ],
        "unii": [
          "K679OBS311"
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      },
      "product_type": "Drugs",
      "event_id": "89836",
      "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 within theUSA",
      "recall_number": "D-0717-2022",
      "product_description": "TheraTears Extra (sodium carboxymethylcellulose) 0.25% Lubricant Eye Drops, 30 Sterile Single-Use Vials per box, Akorn Consumer Health, A Division of Akorn, Inc., Ann Arbor, MI 48105. NDC 58790-010-30",
      "product_quantity": "62,331 box",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20210908",
      "center_classification_date": "20220324",
      "termination_date": "20230928",
      "report_date": "20220330",
      "code_info": "Lot #: 913012, 913013, 913014, Exp. Date 1/31/2023"
    }
  ]
}