{
  "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": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Gurnee",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90720",
      "recalling_firm": "Akorn, Inc",
      "address_1": "5605 Centerpoint Ct Ste B",
      "address_2": "",
      "postal_code": "60031-5278",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed Nationwide in the USA",
      "recall_number": "D-1471-2022",
      "product_description": "Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials, Rx Only, Sterile, Manufactured for:  Akorn, Inc., Lake Forest, IL 60045.  NDC 17478-189-24",
      "product_quantity": "5,226 Cartons (60 vials/carton)",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: Identification of an unknown impurity at the 12-month stability point.",
      "recall_initiation_date": "20220808",
      "center_classification_date": "20220829",
      "report_date": "20220907",
      "code_info": "Lot #: 9N72, EXP 09/30/2022",
      "more_code_info": ""
    }
  ]
}