{
  "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": "2026-04-15",
    "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": "84796",
      "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": "E-Mail",
      "distribution_pattern": "International distribution in the countries of Austria, Germany, Netherlands, Norway, Poland, Switzerland",
      "recall_number": "Z-1342-2020",
      "product_description": "Ambulance Parameter Extension (APE) kit M4758A, an accessory to the Philips HeartStart MRx Monitor/Defibrillator - Product Usage: is intended to be used with the M3536A MRx in EMS environments.",
      "product_quantity": "43 units",
      "reason_for_recall": "M4758A Ambulance Parameter Extension (APE) kit may cause ECG \"Leads Off\" condition in hot, humid environments",
      "recall_initiation_date": "20200114",
      "center_classification_date": "20200221",
      "termination_date": "20210209",
      "report_date": "20200304",
      "code_info": "All"
    }
  ]
}