{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Utica",
      "address_1": "525 French Rd",
      "reason_for_recall": "Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure",
      "address_2": "",
      "product_quantity": "18,720 units in total",
      "code_info": "Lot Numbers:   Y013114-14 Y04191607 Y061413-09 Y081513-07 Y101212-03  Y020714-08 Y04201507 Y06151504 Y081712-39 Y101413-12  Y021413-09 Y042514-10 Y061914-14 Y082212-13 Y10231528  Y021712-01 Y042712-06 Y06261516 Y08281506 Y10231529  Y030113-12 Y05041703 Y071213-13 Y090313-12 Y110714-08  Y03041604 Y05081508 Y071814-11 Y091914-13 Y112414-04  Y031414-04 Y051414-07 Y07191604 Y09241503 Y112613-03  Y032513-03 Y052914-08 Y072712-03 Y092612-16 Y112912-13  Y032612-05 Y060412-05 Y07271508 Y100212-01 Y11301601  Y040314-07 Y060713-12 Y080113-05 Y100713-02 Y121714-09  Y040813-01 Y06071704 Y081114-05 Y10071602 Y121813-09  Y041712-02",
      "center_classification_date": "20180324",
      "distribution_pattern": "Worldwide Distribution: US (Nationwide) and countries of: New Zealand, Saudi Arabia, Switzerland, United Arab Emirates Uruguay & Republic of Macedonia (The former Yugoslav Republic of Macedonia).",
      "state": "NY",
      "product_description": "MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo\" Connector, REF/Catalog Number 2602M     Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes provide the conductive interface between the defibrillator and/or the external transcutaneous (non-invasive) cardiac pacemaker and the pediatric patients skin. The electrode is intended for use on pediatric infants whose weight is less than 10 kg. (22 lbs.).",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ConMed Corporation",
      "recall_number": "Z-1177-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79337",
      "termination_date": "20200917",
      "more_code_info": "",
      "recall_initiation_date": "20180223",
      "postal_code": "13502-5945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}