{
  "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 II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63502",
      "recalling_firm": "Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals",
      "address_1": "120 Vintage Dr NE",
      "address_2": "N/A",
      "postal_code": "35811-8216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-010-2013",
      "product_description": "Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL  35811,  NDC 0603-5092-21.",
      "product_quantity": "2,755 bottles",
      "reason_for_recall": "Tablet Separation: Possibility of cracked or split coating on the tablets.",
      "recall_initiation_date": "20121011",
      "center_classification_date": "20121022",
      "termination_date": "20131209",
      "report_date": "20121031",
      "code_info": "Lot C1130511A, Exp 5/13"
    }
  ]
}