{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Huntsville",
      "state": "AL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "76272",
      "recalling_firm": "Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals",
      "address_1": "130 Vintage Dr Ne",
      "address_2": "N/A",
      "postal_code": "35811-8216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0438-2017",
      "product_description": "DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only,  Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56",
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      "reason_for_recall": "Failed Impurities/ Degradation Specifications",
      "recall_initiation_date": "20170116",
      "center_classification_date": "20170124",
      "termination_date": "20170917",
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      "code_info": "Lot # 0000007104; Exp 05/17"
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}