FDANovember 14, 2024device

BD Pyxis CII Safe ES, REF: 1116-00

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

The hazard

Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

10885403512605

Recall history

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

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