FDAFebruary 14, 2023device

BD Pyxis MedStation ES AUX, REF 324

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

The hazard

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

10885403512681

Recall history

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

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BD Pyxis MedStation ES AUX, REF 324 — Recall Details · AllClear