{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Rockaway",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65462",
      "recalling_firm": "Cardio Medical Products",
      "address_1": "385 Franklin Ave",
      "address_2": "N/A",
      "postal_code": "07866-4037",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-1669-2013",
      "product_description": "Cardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG Electrode Rx Only Single Patient Use Only  Manufactured for Cardio Medical Products 385 Franklin Avenue, Suite L Rockaway, New Jersey 07866  www.cardiomedicalproducts.com  (800) 227-3633 (973) 586-9624 FAX    Defibrillator",
      "product_quantity": "657 units",
      "reason_for_recall": "Covidien received customer reports of Arcing/Sparking on the defibrillation electrode leadwire which may affect Cardio Medical Products Inc. defibrillator electrodes Model Number O101.",
      "recall_initiation_date": "20130426",
      "center_classification_date": "20130708",
      "termination_date": "20160815",
      "report_date": "20130717",
      "code_info": "510 K K103159    Part number O101    Lot numbers Y111412-2  Y111912-17  Y020613-03"
    }
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}