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FDADecember 2, 2024device

Change Healthcare 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

175402621000201754026210003717540262100044175402621000511754026210010517540262100129

Recall history

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

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