{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Nashville",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "98766",
      "recalling_firm": "Harrow Eye LLC",
      "address_1": "1a Burton Hills Blvd Ste 200",
      "address_2": "N/A",
      "postal_code": "37215-6187",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0489-2026",
      "product_description": "FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.",
      "product_quantity": "50,900 units",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20260417",
      "center_classification_date": "20260423",
      "report_date": "20260429",
      "code_info": "Lot #: 1X68, 1X69, Exp. Date 05/31/2027.",
      "more_code_info": ""
    }
  ]
}