Medical device recalls Moderate risk

CHANGE HEALTHCARE CANADA COMPANY recalls Horizon Cardiology Hemo. Version 12.2.

Recall date
August 21, 2024
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0127-2025
FDA classification
Class II
Brand / firm
CHANGE HEALTHCARE CANADA COMPANY
Sold / distributed
Worldwide distribution - US Nationwide and the countries of Australia, Canada, Germany, Ireland, Israel, United Kingdom.

Why it was recalled

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 users understanding.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Horizon Cardiology Hemo. Version 12.2.

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