{
  "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": [
    {
      "country": "United States",
      "city": "Lakewood",
      "address_1": "1200 Paco Way",
      "reason_for_recall": "Labeling: Label mix-up - A complaint was received of one bag of Fluconazole Injection, Iso-Osmotic Sodium Chloride Diluent, USP, 2mg/mL, 50 mL found within the package of 100 mL bags.",
      "address_2": "",
      "product_quantity": "1784 bags",
      "code_info": "Lot #: A0A0539, Exp. 05/19",
      "center_classification_date": "20180424",
      "distribution_pattern": "Product was distributed throughout the United States.",
      "state": "NJ",
      "product_description": "Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), package in 100 mL bags, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902, By: Claris Injectables Limited, Sarkhei-Bavla Road, Chacharwadi-Vasna, Ahmedabad, India  382213, NDC 36000-002-10",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Renaissance Lakewood, LLC",
      "recall_number": "D-0696-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "79580",
      "termination_date": "20190814",
      "more_code_info": "",
      "recall_initiation_date": "20180221",
      "postal_code": "08701-5938",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}