FDAJune 24, 2024device

BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9

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

The hazard

Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

10885403512568

Recall history

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

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