{
  "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": "2026-04-29",
    "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": "67857",
      "recalling_firm": "Philips Medical Systems, Inc.",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of IN and WA., and the countries of : CHINA FRANCE GERMANY ITALY MALAYSIA PANAMA SAUDI ARABIA TURKEY and UNITED KINGDOM.",
      "recall_number": "Z-1439-2014",
      "product_description": "Philips HeartStart XL+ Defibrillator/Monitor   Model number: 861290, automatic external defibrillator.",
      "product_quantity": "19 units",
      "reason_for_recall": "A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy",
      "recall_initiation_date": "20140331",
      "center_classification_date": "20140409",
      "termination_date": "20151021",
      "report_date": "20140416",
      "code_info": "Serial Numbers:  USN1307680 USD1309181  USD1308456 USD1309182  USD1309167 USD1309184  USD1309168 USD1309194  USD1309180 USD1309195  USD1309196 USD1309274  USD1309197 USD1309286  USD1309227 USD1309301  USD1309264 US11409686  USD1309269"
    }
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}