{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bothell",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79343",
      "recalling_firm": "Philips Electronics North America Corp.",
      "address_1": "22100 Bothell Everett Hwy",
      "address_2": "N/A",
      "postal_code": "98021-8431",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was nationwide and to Puerto Rico.  There was also government/military distribution.   Foreign distribution was made to the following countries:  Canada, Afghanistan, Algeria, Argentina, Aruba, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Botswana, Brazil, Brunei Darussalam, Cambodia, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Fiji, Finland, France, Georgia, Germany, Ghana, Greece, Guatemala,  Hong Kong, Iceland, India, Indonesia, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Kenya, Republic of Korea, Kuwait, Latvia, Lebanon, Libya, Lithuania, Luxembourg, Macao, Malaysia, Malta, Mauritius, Mexico, Morocco, Namibia, Netherlands, Netherlands Antilles, New Caledonia, New Zealand, Niger, Norway, Oman, State of Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Sri Lanka, Suriname, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirate, United Kingdom, Uzbekistan, Venezuela, Viet Nam, Yemen, Zambia, and Zimbabwe.",
      "recall_number": "Z-1914-2018",
      "product_description": "Philips HeartStart (HS1) Onsite/Home AED",
      "product_quantity": "Total for FRx and HS1 - 660,519 defibrillators",
      "reason_for_recall": "An issue with one of the electric components (a resistor) could result in the device not delivering a shock when needed.",
      "recall_initiation_date": "20180314",
      "center_classification_date": "20180523",
      "termination_date": "20200819",
      "report_date": "20180530",
      "code_info": "Manufactured between September 2002 and February 2013.  The year of manufacture can be identified by the 2nd and 3rd characters in the serial number on the back of the AED in the following ranges:    Home/Onsite: A02x-xxxxx through A13B-xxxxx;  FRx:  B04x-xxxxx through B13B-xxxxx    NOTE:  If the device was manufactured in 2013 and the 4th digit is the letter \"C\" or later (D, E, F...), it is not covered by the recall (i.e. A13G-02375).    In some cases, a device within the date range covered by the notification did not contain a resistor previously associated with a failure.  In that case, a notification was not sent.  Confirmation as to whether the device contains the resistor at issue can be done by contacting the firm."
    }
  ]
}