{
  "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": "Andover",
      "address_1": "3000 Minuteman Road",
      "reason_for_recall": "Defibrillator/monitor cannot analyze an ECG report during acquisition of 12 lead ECG",
      "address_2": "",
      "product_quantity": "35 units",
      "code_info": "Serial Numbers:  US00558452, US00558453, US00558493, US00558494, US00558539 US00558540, US00558546, US00558547, US00558569, US00558576 US00558584, US00558595, US00558596, US00558597, US00558615  US00558617, US00558618, US00558619, US00558620, US00558621  US00558625, US00558626, US00558627, US00558628, US00558629  US00558630, US00558640, US00558641, US00558642, US00558643  US00558644, US00558779, US00558780, US00558950, US00558952",
      "center_classification_date": "20120711",
      "distribution_pattern": "Worldwide Distribution - USA including FL, IN, MA, M, NY, OH, TN, TX, and VA.  Internationally to AUSTRALIA, HONG KONG, and INDIA",
      "state": "MA",
      "product_description": "Philips HeartStart MRx M3536A Defibrillator/Monitor with Software R.03.03    The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician",
      "report_date": "20120718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare Inc.",
      "recall_number": "Z-1986-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62342",
      "termination_date": "20130814",
      "more_code_info": "",
      "recall_initiation_date": "20120620",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}