{
  "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": "Redmond",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76162",
      "recalling_firm": "Physio-Control, Inc.",
      "address_1": "11811 Willows Rd NE",
      "address_2": "N/A",
      "postal_code": "98052-2003",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  LifePak 12 distributed in US states of AL, GA, NY, SC, and in Australia.    LifePak 15 distributed nationwide in the US including Puerto Rico and to  ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, CANADA, CHILE, CZECH REPUBLIC, DENMARK, FINLAND, FRANCE, FRENCH GUIANA, GERMANY, GREECE, HUNGARY, ICELAND, IRELAND, ITALY, LITHUANIA, LUXEMBOURG, NETHERLANDS, NEW ZEALAND, NORWAY, POLAND, PORTUGAL, SAUDI ARABIA, SENEGAL, SERBIA, SLOVENIA, SOUTH AFRICA, SPAIN, SWITZERLAND, TAHITI, UNITED ARAB EMIRATES, AND UNITED KINGDOM.",
      "recall_number": "Z-1143-2017",
      "product_description": "LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option.     The device is used in various areas of the hospital such as critical areas (emergency departments, critical care, operating room, etc.) and general duty floors (e.g. medical/surgical).     The device is also used for in and out of hospital transport (air and ground ambulance, in hospital transport, etc.)",
      "product_quantity": "7 units in the US and 13 modules worldwide (5 international; and 8 owned by Physio)",
      "reason_for_recall": "The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX after start-up or during device operation.",
      "recall_initiation_date": "20170116",
      "center_classification_date": "20170207",
      "termination_date": "20180911",
      "report_date": "20170215",
      "code_info": "LOT NUMBERS  OF AFFECTED MODULE: Lot # 1520 and 1544.    SERIAL NUMBERS OF DEVICES:    32877820, 34356891, 35984435, 37223110, 37440401, 37456675, and 37913307."
    }
  ]
}