{
  "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": "Huntsville",
      "address_1": "120 Vintage Dr NE",
      "reason_for_recall": "Failed Dissolution Specifications: During routine stability testing  at the 12 month time point, one product lot was found to be  out of specification for dissolution.",
      "address_2": "",
      "product_quantity": "2016 bottles",
      "code_info": "Lot #: T142A14A, T143A14A, T144A14A, Exp 01/16",
      "center_classification_date": "20150630",
      "distribution_pattern": "Nationwide",
      "state": "AL",
      "product_description": "Disulfiram tablets, USP, 500 mg, 100-count bottles, Rx only, Manufactured for and by Qualitest Pharmaceuticals 130 Vintage Drive Huntsville, AL  35811. NDC 0603-3432-21.",
      "report_date": "20150708",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Qualitest Pharmaceuticals",
      "recall_number": "D1151-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "71563",
      "termination_date": "20161023",
      "more_code_info": "",
      "recall_initiation_date": "20150618",
      "postal_code": "35811-8216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}