{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Richmond",
      "state": "",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95284",
      "recalling_firm": "CHANGE HEALTHCARE CANADA COMPANY",
      "address_1": "10711 Cambie Rd Suite 130",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Australia, Canada, Germany, Ireland, Israel, United Kingdom.",
      "recall_number": "Z-0127-2025",
      "product_description": "Horizon Cardiology Hemo. Version 12.2.",
      "product_quantity": "3 systems",
      "reason_for_recall": "A potential issue has been identified in Change Healthcare Cardiology Hemo where incorrect data entry can lead to inaccurate hemodynamic calculations, potentially resulting in misdiagnosis and inappropriate treatment. This issue occurs when the unit of measurement (UOM) for hemoglobin is configured in a way that differs from the user\u0019s understanding.",
      "recall_initiation_date": "20240821",
      "center_classification_date": "20241017",
      "report_date": "20241023",
      "code_info": "No UDI. Version 12.2",
      "more_code_info": ""
    }
  ]
}