{
  "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": "2026-04-01",
    "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": "84115",
      "recalling_firm": "Philips North  America, LLC",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide",
      "recall_number": "Z-0498-2020",
      "product_description": "HeartStart XL+ Defibrillator/Monitor, Model 861290",
      "product_quantity": "23,749 Units",
      "reason_for_recall": "The rotary therapy selector switch may fail, resulting in unexpected device behavior. These behaviors include:  The device may not turn on; The device may not perform the selected function; The device may deliver a shock with an energy level different from the setting selected by the user.",
      "recall_initiation_date": "20191016",
      "center_classification_date": "20191119",
      "termination_date": "20231129",
      "report_date": "20191127",
      "code_info": "All units manufactured prior to 1 May 2017."
    }
  ]
}