{
  "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": [
    {
      "status": "Terminated",
      "city": "Belfast",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63139",
      "recalling_firm": "Heartsine Technologies, Limited",
      "address_1": "203 Airport Road West",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution and US (nationwide) in the following states:  AK, AL, AP, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, WA, and WI.",
      "recall_number": "Z-0124-2013",
      "product_description": "HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753; 10C00200000 to 10C00210106    Product Usage: Samaritan 300/300P PAD  is indicated for use on victims of sudden cardiac arrest who are exhibiting the following signs:  Unconsciousness  Not breathing  Without circulation",
      "product_quantity": "81,982 in total",
      "reason_for_recall": "Certain Samaritan 300/300P PAD devices may experience one or both of the following conditions that could affect the ability to deliver therapy to a patient in an SCA event if needed:  Issue 1 (On/Off Issue):  the device may turn itself on and off without input from the user.  When this occures, the normal sequence of audible instruction prompts that occurs when the device is turned on will be emit",
      "recall_initiation_date": "20120913",
      "center_classification_date": "20121026",
      "termination_date": "20150710",
      "report_date": "20121107",
      "code_info": "Serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753; 10C00200000 to 10C00210106",
      "more_code_info": ""
    }
  ]
}