{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71963",
      "recalling_firm": "Covidien LLC",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  Canada  Australia  Denmark  Germany  New Zealand",
      "recall_number": "Z-2547-2015",
      "product_description": "Physio-Control Quik\u0010Combo Pacing/Defibrillation/ECG Electrodes Redi\u0010Pak¿ Preconnect System  Item Code:PM20022",
      "product_quantity": "56,000 sets",
      "reason_for_recall": "Multi-Function Defibrillation Electrodes, Pre connect-  potential for damage to the wire insulation may    result in a potentially increased risk for reduced or no patient therapy and patient and/or clinician burns",
      "recall_initiation_date": "20150819",
      "center_classification_date": "20150902",
      "termination_date": "20170524",
      "report_date": "20150909",
      "code_info": "Lot Numbers:  516907, 519815, 519816"
    }
  ]
}