{
  "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": [
    {
      "status": "Terminated",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65334",
      "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-599-2013",
      "product_description": "Fentanyl Transdermal System, 50 mcg/h, 1 system per pouch (NDC 0591-3212-54), packaged in 5-count systems per box (NDC 0591-3212-72), Rx only, Manufactured by Watson Laboratories, Inc, Corona, CA, 92880 USA; Distributed by: Watson Pharma, Inc.",
      "product_quantity": "98,952 boxes",
      "reason_for_recall": "Failed Impurities/Degradation Specifications",
      "recall_initiation_date": "20130603",
      "center_classification_date": "20130612",
      "termination_date": "20140409",
      "report_date": "20130619",
      "code_info": "Lot #: Patch 453658; Carton 453658A, Exp 09/13"
    }
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}