{
  "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 Rd",
      "reason_for_recall": "Device Operating on Battery Power May Shutdown without Warning if exposed to elevated levels of electromagnetic interference from other radio frequency (RF) energy sources and",
      "address_2": "",
      "product_quantity": "64,972",
      "code_info": "Serial numbers ranging:   From US00100100 to US00210461",
      "center_classification_date": "20131231",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to the following countries:  AFGHANISTAN  ALBANIA  ARGENTINA  ARUBA  AUSTRALIA  AUSTRIA  AZERBAIJAN  BAHRAIN  BANGLADESH  BELGIUM  BOLIVIA  BOSNIA AND HERZEGOWINA  BRAZIL  BRUNEI DARUSSALAM  BULGARIA  CAMBODIA  CANADA  CHILE  CHINA  COLOMBIA  COSTA RICA  CROATIA (local name: Hrvatska)  CYPRUS  CZECH REPUBLIC  DENMARK  ECUADOR  EGYPT  EL SALVADOR  ESTONIA  ETHIOPIA  FINLAND  FRANCE  GERMANY  GREECE  GUADELOUPE  HONG KONG  ICELAND  INDIA  INDONESIA  IRAQ  IRELAND  ISRAEL  ITALY  JAPAN  JORDAN  KAZAKHSTAN  KENYA  KOREA, REPUBLIC OF  KUWAIT  LAOS  LATVIA  LEBANON  LIBYAN ARAB JAMAHIRIYA  LITHUANIA  LUXEMBOURG  MACAU  MACEDONIA  MALAYSIA  MALTA  MEXICO  MONGOLIA  MOROCCO  NAMIBIA  NEPAL  NETHERLANDS  NETHERLANDS ANTILLES  NEW CALEDONIA  NEW ZEALAND  NICARAGUA  NIGERIA  NORWAY  OMAN  PAKISTAN  PALESTINE  PANAMA  PAPUA NEW GUINEA  PARAGUAY  PERU  PHILIPPINES  POLAND  PORTUGAL  PUERTO RICO  QATAR  REUNION  ROMANIA  RUSSIAN FEDERATION  SAUDI ARABIA  SERBIA  SINGAPORE  SLOVENIA  SOUTH AFRICA  SPAIN  SRI LANKA  SWEDEN  SWITZERLAND  TAIWAN, PROVINCE OF CHINA  TANZANIA, UNITED REPUBLIC OF  THAILAND  TRINIDAD AND TOBAGO  TUNISIA  TURKEY  TURKMENISTAN  UGANDA  UKRAINE  UNITED ARAB EMIRATES  UNITED KINGDOM  UZBEKISTAN  VENEZUELA  VIET NAM  YEMEN",
      "state": "MA",
      "product_description": "Philips HeartStart MRx Monitor/Defibrillator  Models: M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6  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": "20140108",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems, Inc.",
      "recall_number": "Z-0613-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67035",
      "termination_date": "20170413",
      "more_code_info": "",
      "recall_initiation_date": "20130410",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}