{
  "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": [
    {
      "country": "United States",
      "city": "Miami",
      "address_1": "11960 Sw 144th St",
      "reason_for_recall": "Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the release liner from the patch adhesive prior to administration.",
      "address_2": "",
      "product_quantity": "242,100 patches",
      "code_info": "Lot #: 43008, Exp 01/12; 48591, Exp 10/12",
      "center_classification_date": "20120614",
      "distribution_pattern": "Nationwide and Puerto Rico.",
      "state": "FL",
      "product_description": "Daytrana (methylphenidate) transdermal system patch, Delivers 30 mg over 9 hours (3.3 mg/hr), 1 patch per pouch (NDC 54092-555-01), packaged in 30-count patches per box (NDC 54092-555-30), Rx only, Manufactured for Shire US Inc., Wayne, PA 19087 by Noven Pharmaceuticals, Inc., Miami, FL 33186.",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Noven Pharmaceuticals, Inc.",
      "recall_number": "D-1373-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "61891",
      "termination_date": "20130523",
      "more_code_info": "",
      "recall_initiation_date": "20110705",
      "postal_code": "33186-6109",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}