Reported Jan 22, 2025 · Ongoing
McKesson Cardiology Hemo software
A L I Technologies Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: A L I Technologies Ltd · 3700 Gilmore Way Suite 207 · Burnaby · N/A
Is this the product you have?
- McKesson Cardiology Hemo software
- Lot codes and dates
- Software versions
13.1.2/No UDI13.2.1/UDI:(01)8001093905001014/(01)80010939050027
- Software versions
- Amount recalled
- 1 unit
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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