{
  "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": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64201",
      "recalling_firm": "Philips Healthcare Inc.",
      "address_1": "3000 Minuteman Road",
      "address_2": "N/A",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally  to ALGERIA, ANGOLA, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, BULGARIA, COLOMBIA, CROATIA (LOCAL NAME HYVATSKA), CYPRUS, CZECH REPUBLIC, DENMARK, DOMINICAN REPUBLIC, EGYPT, ESTONIA, FINLAND, FRANCE, GABON, GERMANY, HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRAN (ISLAMIC REPUBLIC OF), IRAQ, IRELAND, ISRAEL, ITALY, JORDAN, KENYA, REPUBLIC OF KOREA, KUWAIT, LATVIA, LEBANON, LIBYAN ARAB JAMAHIRIYA, LITHUANIA, MALAYSIA, MALTA, MAURITIUS, MOROCCO, NAMIBIA, NETHERLANDS, NEW ZEALAND, NORWAY, OMAN, PALESTINE, POLAND, PORTUGAL, ROMANIA, SAUDI ARABIA, SINGAPORE, SLOVAKIA (SLOVAK REPUBLIC), SLOVENIA, SOUTH AFRICA, SPAIN, SRI LANKA, SWEDEN, SWITZERLAND, SYRIAN ARAB REPUBLIC, TANZANIA, THAILAND, TRINIDAD AND TOBAGO, TUNISIA, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, AND VIET NAM.",
      "recall_number": "Z-0871-2013",
      "product_description": "Philips HeartStart XL+ Defibrillator/Monitor   Model number: 861290    The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation",
      "product_quantity": "3785 units",
      "reason_for_recall": "Philips HeartStart XL+ Defibrillator/Monitor may become locked out of clinical use",
      "recall_initiation_date": "20130128",
      "center_classification_date": "20130221",
      "termination_date": "20200903",
      "report_date": "20130227",
      "code_info": "Serial number range:  USO1100100 - USO1100372,   USN1100376 - USN1100960,  USD1100961 - USD1101095,   US11201096 - US11201186,   US21201187 - US21201239,   US31201240 - US31201537,   US41201538 - US41201585,   US51201586 - US51201721,   US61201722 -US61201924,   US71201925 - US71202048,   US81202049 - US81202168,  US91202169- US91202514,   USO1202515 - USO1202990,   USN1202991 - USN1203537,   USD1203538- USD1203968,   US11303969 - US11303972"
    }
  ]
}