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Official recall record

Change Healthcare Cardiology Hemo/Hemodynamics™

Health Canada — Medical Devices · 2025-06-05 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-06-05
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

A recent software modification introduced to enhance application stability inadvertently caused unintended regressions in the user experience. The modification was designed to provide a robust solution for dealing with applications freezes. While this approach aimed to improve overall system reliability and stability, it has led to isolated scenarios where the application aborts unexpectedly during specific workflows. In the Change Healthcare Cardiology Hemo product, this regression manifests as localized failures of the Hemo Infosystem application during certain workflows. These occurrences are limited to specific use cases and do not affect the broader functionality of the product. The real time monitor continues to operate and provide patient monitoring information to the user. Recall start date: May 22, 2025

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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