{
  "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": "Philips MRx devices have an EtCO2 module that may contain contamination; this contamination (will/may) cause the device to be unable to display the EtCO2 or CO2 waveform (capnogram).",
      "address_2": "",
      "product_quantity": "20 units  ( 18 domestic, 2 foreign)",
      "code_info": "20 units - US00597060, US00597964, US00598048, US00598210, US00598784, US00599490, US00599495, US00599508, US00599572, US00599613, US00599615, US00599623, US00599726, US00600362, US00600363, US00600370, US00600422, US00600423, US00600438, US00600483",
      "center_classification_date": "20171221",
      "distribution_pattern": "20 units affected.  18 domestic, 2 foreign.",
      "state": "MA",
      "product_description": "Automated External Defibrillator - HeartStart MRx Monitor/Defibrillator",
      "report_date": "20171227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Electronics North  America Corporation",
      "recall_number": "Z-0278-2018",
      "initial_firm_notification": "",
      "product_type": "Devices",
      "event_id": "78698",
      "termination_date": "20181012",
      "more_code_info": "",
      "recall_initiation_date": "20170928",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}