{
  "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": "Deerfield",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83103",
      "recalling_firm": "Cardiac Science Corporation",
      "address_1": "500 Burdick Pkwy",
      "address_2": "N/A",
      "postal_code": "53531-9692",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US distribution to Georgia, Texas, and Wisconsin.",
      "recall_number": "Z-1938-2019",
      "product_description": "Powerheart¿ G5 Automatic AED",
      "product_quantity": "5 devices",
      "reason_for_recall": "Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications.",
      "recall_initiation_date": "20190604",
      "center_classification_date": "20190703",
      "termination_date": "20211115",
      "report_date": "20190710",
      "code_info": "Model Number G5A 80A;     AED Serial Number (UDI Number):  D00000133922 )(01)00812394021222(11)190508(21)D00000133922), D00000133927 ((01)00812394021222(11)190509(21)D00000133927), D00000133930 ((01)00812394021222(11)190509(21)D00000133930), D00000133934 ((01)00812394021222(11)190509(21)D00000133934), D00000133936 )(01)00812394021222(11)190509(21)D00000133936)."
    }
  ]
}