A L I Technologies recalls software version 15.01/UDI:(01)17540:129 due to potential incorrect medication administration. Affected healthcare providers should verify software version.
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
A L I Technologies recalls its Change Healthcare Cardiology Hemodynamics software version 15.01/UDI:(01)17540262100129 because a software defect in the autosave mechanism could lead to clinicians administering incorrect medications. This recall affects healthcare providers using the software for hemodynamics monitoring.
The software has a defect in its autosave mechanism that may cause clinicians to administer incorrect medications. This happens because the software fails to properly save patient data, leading to potential medication errors during treatment.
Healthcare providers using the Change Healthcare Cardiology Hemodynamics software for hemodynamics monitoring are most at risk. This recall specifically impacts users of the affected software version.
Check if you have the software version 15.01 with UDI code (01)17540262100129. The software is used for hemodynamics monitoring in healthcare settings.
Check your software version to confirm it is 15.01/UDI:(01)17540262100129.
Yes, the software has a defect that could lead to incorrect medication administration, which may cause serious harm.
Verify your software version. If it matches the recalled version, contact A L I Technologies for further instructions.
Check for software version 15.01 with UDI code (01)17540262100129 in your healthcare system.
We’ve drafted a message you can send A L I Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0959-2025 — A L I Technologies A L I Technologies Hello, I own a A L I Technologies that is covered by recall Z-0959-2025 from A L I Technologies. 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.
