FDADecember 12, 2022device

BD Pyxis MedBank System - Product Label/labeling pending

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

The hazard

Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

1088540351256810885403512544108854035127041119001139001088540351381710885403513794

Recall history

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

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