{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mansfield",
      "address_1": "15 Hampshire Street",
      "reason_for_recall": "Defibrillation  Electrodes may arc/spark result in thermal damage to the leadwire, which could render the device incapable of delivering the appropriate energy or shock to the patient",
      "address_2": "",
      "product_quantity": "133470 (sets of 2)",
      "code_info": "Lot Numbers:  226543X,  230054X , 230814X,   232182X, 232805X,   234245X,  304667X,   301844X,  300446X, 305320X",
      "center_classification_date": "20130429",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Korea, Japan, Canada, Australia, Brazil, Belgium, Singapore, and South Africa.",
      "state": "MA",
      "product_description": "Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode  Product ID: 22550R.    Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.",
      "report_date": "20130508",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Covidien LLC",
      "recall_number": "Z-1184-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64868",
      "termination_date": "20151119",
      "more_code_info": "",
      "recall_initiation_date": "20130408",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}