{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Los Angeles",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "84978",
      "recalling_firm": "Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical",
      "address_1": "1990 Westwood Blvd Ste 135",
      "address_2": "N/A",
      "postal_code": "90025-4650",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "U.S.A. Nationwide and Puerto Rico, Barbados and Dominican Republic",
      "recall_number": "D-0951-2020",
      "product_description": "Dexamethasone (LA) Injectable Suspension, DEXAMETHASONE LA [10ML] 16MG  INJ SUSP, For IM, IA Use, Shake Well, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0630-1",
      "product_quantity": "N/A",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20200115",
      "center_classification_date": "20200305",
      "termination_date": "20231207",
      "report_date": "20200311",
      "code_info": "Lot #: 10022019+53002, Exp 10/1/2020"
    }
  ]
}