FDADecember 2, 2024device

McKesson Cardiology Hemo software

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).

What to do

FDA enforcement status: Ongoing

Brands named

l i technologies

UPCs

8001093905001080010939050027

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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McKesson Cardiology Hemo software — Recall Details · AllClear