{
  "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": "Update XL¿ device software to  version A.03.  This includes enhancements to the Operational Checks, event logs, and troubleshooting messages that provide as complete of information as needed to users on  device readiness.",
      "address_2": "",
      "product_quantity": "4315",
      "code_info": "HeartStart XL+ Defibrillator/Monitor,All Chinese XL  manufactured before September, 2017, unless the XL+ is affected by F5N86100172, and has not been updated.",
      "center_classification_date": "20180313",
      "distribution_pattern": "Foreign Only - China",
      "state": "MA",
      "product_description": "HeartStart XL+ Defibrillator/Monitor    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. It must be used by or on the order of a physician. When operating as a semi-automatic external defibrillator in AED Mode, the HeartStart XL+ is suitable for use by medical personnel trained in basic life support that includes use of an AED. When operating in Monitor, Manual Defib, or Pacer Mode, the HeartStart XL+ is suitable for use by healthcare professionals trained in advanced life support.",
      "report_date": "20180321",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Philips Electronics North  America Corporation",
      "recall_number": "Z-0978-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79191",
      "termination_date": "20200207",
      "more_code_info": "",
      "recall_initiation_date": "20180207",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}