{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Wuxi",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98917",
      "recalling_firm": "GE Medical Systems China Co., Ltd.",
      "address_1": "No. 19 Changjiang Road",
      "address_2": "Development Zone National Hi-Tech Xin District",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of Florida and Georgia. The countries of India, Italy, Republic of Korea, and United Kingdom.",
      "recall_number": "Z-2306-2026",
      "product_description": "MAC 5 A4 Resting ECG Analysis System 855001-001;  MAC 5 A5 Resting ECG Analysis System 8855002-001.  Electrocardiograph",
      "product_quantity": "16",
      "reason_for_recall": "Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.",
      "recall_initiation_date": "20260421",
      "center_classification_date": "20260603",
      "report_date": "20260610",
      "code_info": "Software version 3.00  855001-001, UDI-DI 00195278276070  8855002-001, UDI-DI 00195278276124",
      "more_code_info": ""
    }
  ]
}