Change Healthcare Cardiology Hemo software versions 14.2, 14.1.1, 14.3, 15.0.1, and 15.1 may cause inaccurate hemodynamic calculations due to hemoglobin unit configuration errors, risking misdiagnosis.
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.
Change Healthcare Cardiology Hemo software versions 14.2, 14.1.1, 14.3, 15.0.1, and 15.1 have been recalled because incorrect hemoglobin unit configuration can lead to inaccurate hemodynamic calculations. This could result in misdiagnosis and inappropriate treatment for patients using the software.
The software may misconfigure the unit of measurement for hemoglobin, causing hemodynamic calculations to be inaccurate. This could lead to incorrect medical decisions and potentially inappropriate patient treatment.
Healthcare providers using the affected software versions are most at risk, as incorrect hemoglobin data entry could lead to misdiagnosis and inappropriate treatment.
Check if your software version is listed: 14.2, 14.1.1, 14.3, 15.0.1, or 15.1. The UDI numbers are also listed in the recall notice.
Identify your software version by checking the device or software settings.
Versions 14.2, 14.1.1, 14.3, 15.0.1, and 15.1 are affected.
Incorrect hemoglobin unit configuration can lead to inaccurate hemodynamic calculations, potentially causing misdiagnosis and inappropriate treatment.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Change Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0126-2025 — Change Healthcare Change Healthcare Hello, I own a Change Healthcare that is covered by recall Z-0126-2025 from Change Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
