A L I Technologies recalls specific Hemo software versions due to a defect that may cause clinicians to administer incorrect medications. Affected versions include 14.1.1 through 15.1.
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
A L I Technologies recalls certain versions of their Hemo software because a defect in the autosave feature could lead to clinicians giving the wrong medications. This is serious because medication errors can cause harm to patients during medical procedures.
The software defect causes the autosave mechanism to malfunction, potentially leading to clinicians administering incorrect medications. This risk occurs during medical procedures where precise medication dosing is critical.
Healthcare providers using the recalled software versions are most at risk. Patients receiving care from these systems could be affected if incorrect medications are administered.
Check if your software version matches the listed numbers: 14.1.1/(01)17540262100020, 14.2/(01)17540262100037, 14.3/(01)17540262100044, 14.3.2/(01)17540262100051, 15.01/(01)17540262100105, or 15.1/(01)17540262100129.
Identify your software version by checking the version number and unique identifier (UDI) listed in the recall notice.
The affected versions are 14.1.1/(01)17540262100020, 14.2/(01)17540262100037, 14.3/(01)17540262100044, 14.3.2/(01)17540262100051, 15.01/(01)17540262100105, and 15.1/(01)17540262100129.
The recall does not specify an immediate stop-use action; however, healthcare providers should check their software version and take corrective steps if affected.
The recall notice does not provide a remedy, so affected users should contact A L I Technologies for guidance on resolving the issue.
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-0958-2025 — A L I Technologies A L I Technologies Hello, I own a A L I Technologies that is covered by recall Z-0958-2025 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.
