{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62384",
      "recalling_firm": "Actavis",
      "address_1": "575/577/579 Chipeta Way",
      "address_2": "N/A",
      "postal_code": "84108-1222",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1693-2012",
      "product_description": "Fentanyl Transdermal System, 100 mcg/h, each transdermal system contains: 10 mg fentanyl and 0.4 mL alcohol USP, Rx only, supplied in single pouches (NDC 0591-3214-54 (pouch)), 5 pouches per carton (NDC 0591-3214-72 (Carton)), Manufactured by Watson laboratories Inc., Corona, CA, Distributed by: Watson, Pharma Inc.",
      "product_quantity": "98,088 cartons (5 pouches per carton)",
      "reason_for_recall": "Subpotent; some patches may not contain fentanyl gel",
      "recall_initiation_date": "20120711",
      "center_classification_date": "20120925",
      "termination_date": "20130410",
      "report_date": "20121003",
      "code_info": "Lot number 455040A (carton) 455040 (pouch)",
      "more_code_info": ""
    }
  ]
}