{
  "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": "Terminated",
      "city": "New Castle",
      "state": "DE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65967",
      "recalling_firm": "Marlex Pharmaceuticals, Inc.",
      "address_1": "50 McCullough Dr",
      "address_2": "Southgate Industrial Park",
      "postal_code": "19720-2066",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-1064-2013",
      "product_description": "Acetaminophen Tablets, 500 mg, 100-count bottles, Distributed by: Marlex Pharmaceuticals, Inc., New Castle, DE  19720, List No. 152, NDC 10135-152-01, UPC 3 10135 15201 8.",
      "product_quantity": "28,387 bottles",
      "reason_for_recall": "CGMP Deviations: The recalled acetaminophen tablet lot was not manufactured under current good manufacturing practices as noted by a recent inspection of the manufacturing firm.",
      "recall_initiation_date": "20130808",
      "center_classification_date": "20130927",
      "termination_date": "20141120",
      "report_date": "20131009",
      "code_info": "Lot #: 3213, Exp 12/13",
      "more_code_info": ""
    }
  ]
}