A L I Technologies recalls McKesson Cardiology Hemo software versions 13.1.2, 13.2.1, and 14 due to a software defect that may cause clinicians to administer incorrect medications.
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
A L I Technologies recalls specific versions of McKesson Cardiology Hemo software because a defect in the autosave mechanism could lead to clinicians giving the wrong medications. This is serious because medication errors could harm patients during medical procedures.
The software defect affects the autosave mechanism, which may cause clinicians to accidentally administer incorrect medications. This happens because the software fails to properly save or verify medication selections before use, leading to potential medication errors.
Healthcare providers using the recalled software versions are most at risk, as incorrect medication administration could occur during clinical procedures.
Check the software version number on your device. Recalled versions include 13.1.2 (no UDI), 13.2.1 (UDI: 0180010939050010), and 14 (UDI: 0180010939050027).
Identify your software version by checking the device settings or documentation. Recalled versions are 13.1.2, 13.2.1, and 14.
Contact A L I Technologies for updated software versions to fix the autosave defect and prevent medication errors.
Recalled versions are 13.1.2 (no UDI), 13.2.1 (UDI: 0180010939050010), and 14 (UDI: 0180010939050027).
The software defect may cause clinicians to administer incorrect medications during procedures, which could harm patients.
No, but you should update to a fixed version to prevent medication errors. The recall does not require immediate discontinuation.
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-0957-2025 — A L I Technologies A L I Technologies Hello, I own a A L I Technologies that is covered by recall Z-0957-2025 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.
