Official recall record
Change Healthcare Cardiology Hemo/Hemodynamics™
- 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.
Record last checked against the registry on 2026-05-31.