{
  "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 I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76252",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and in the following countries: Bahrain, Belize, Cambodia, Chile, China, C¿te d'Ivoire, Ecuador, Germany, Honduras, Hong Kong, India, Indonesia, Jamaica, Myanmar, Netherlands, Niger, Philippines, Saudi Arabia, Senegal, Singapore, Sri Lanka, Thailand, Tunisia, Ukraine, and Zambia.",
      "recall_number": "Z-1257-2017",
      "product_description": "The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.",
      "product_quantity": "total 133,330 units (50,046 units in the US)",
      "reason_for_recall": "The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.",
      "recall_initiation_date": "20170113",
      "center_classification_date": "20170303",
      "termination_date": "20190822",
      "report_date": "20170315",
      "code_info": "Affected Product Part Numbers: 320371500XX.  There are 133,330 affected serial numbers."
    }
  ]
}