{
  "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": [
    {
      "status": "Ongoing",
      "city": "Huntsville",
      "state": "AL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63138",
      "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": "Press Release",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-057-2013",
      "product_description": "HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for:  QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-3888-21",
      "product_quantity": "14,445 bottles",
      "reason_for_recall": "Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components.",
      "recall_initiation_date": "20120910",
      "center_classification_date": "20121116",
      "report_date": "20121128",
      "code_info": "Lot number: C1440512A, Exp 12/13"
    }
  ]
}