McKesson Cardiology Hemo software version 13.0 may not display physiological signals under certain conditions. Affected units were sold for clinical monitoring and data processing. Contact McKesson for remedy.
Change Healthcare has identified an issue where, under certain circumstances, the Real Time Monitor (RTM) may not display physiological signals.
McKesson Cardiology Hemo software version 13.0 may not display physiological signals under certain conditions. This could affect patient monitoring accuracy in clinical settings. Users should check their software version and contact the manufacturer for assistance.
The software may fail to display physiological signals under specific conditions, potentially leading to inaccurate patient monitoring. This could impact clinical decision-making if critical data is not visible. However, the issue is limited to software functionality and not a physical hazard.
Healthcare providers using McKesson Cardiology Hemo software version 13.0 for patient monitoring and clinical data processing are most at risk. Patients using this system for physiological monitoring may be affected if signals are not displayed correctly.
Check for software version 13.0 HF1, 13.0HF2, or 13.0HF3 on the device. The product is used for physiological monitoring and clinical data processing in healthcare settings.
Verify your software version is 13.0 HF1, 13.0HF2, or 13.0HF3.
Software versions 13.0 HF1, 13.0HF2, and 13.0HF3.
The software may not display physiological signals under certain conditions, which could affect patient monitoring accuracy.
Check your software version and contact McKesson for assistance.
We’ve drafted a message you can send McKesson Cardiology Hemo to request your refund or repair — edit it as you like.
Subject: Recall Z-2968-2018 — McKesson Cardiology Hemo McKesson Cardiology Hemo Hello, I own a McKesson Cardiology Hemo that is covered by recall Z-2968-2018 from McKesson Cardiology Hemo. 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.
