{
  "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": [
    {
      "country": "United States",
      "city": "Chadds Ford",
      "address_1": "100 Endo Blvd",
      "reason_for_recall": "Adulterated Presence of Foreign Tablets: Customer complaint that some Endocet 10 mg/325 mg tablets were found mixed in a bottle with Endocet 10 mg/650 mg tablets.",
      "address_2": "",
      "product_quantity": "11,764 bottles",
      "code_info": "Lot #: 402794NV, Exp 12/13",
      "center_classification_date": "20120614",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "state": "PA",
      "product_description": "Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured for: Endo Pharmaceuticals Inc., Chadds Ford, PA, By: Novartis, Lincoln, NE  68501; NDC 60951-797-70.",
      "report_date": "20120620",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Endo Pharmaceuticals, Inc.",
      "recall_number": "D-1381-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "61791",
      "termination_date": "20130621",
      "more_code_info": "",
      "recall_initiation_date": "20120507",
      "postal_code": "19317",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}