{
  "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": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "76421",
      "recalling_firm": "Actavis Inc",
      "address_1": "400 Interpace Pkwy",
      "address_2": "N/A",
      "postal_code": "07054-1120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0514-2017",
      "product_description": "Levofloxacin Ophthalmic Solution, 0.5%, Sterile,  packaged in 5mL bottles, Rx Only, Manufactured by  Hi-Tech Pharmacal Co., Inc., Amityville, NY 11707, NDC 50383-283-05",
      "product_quantity": "14280 bottles",
      "reason_for_recall": "Failed Impurities/ Degradation Specifications: OOS for related compound (levofloxacin n-oxide) at the 18  month stability time point.",
      "recall_initiation_date": "20170207",
      "center_classification_date": "20170309",
      "termination_date": "20180109",
      "report_date": "20170315",
      "code_info": "Lot # 348748, Exp 11/30/2017; 350578, Exp 3/31/2018; 633467, Exp 3/31/2017"
    }
  ]
}