FDAClass IIJanuary 29, 2025

BD Pyxis Med 4000 Auxiliary recall

BD Pyxis Med 4000 Auxiliary (AUX), REF 314

Why was BD Pyxis Med 4000 Auxiliary recalled?

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 should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 10885403512650, Serial Numbers: 16140589, 16194078, 16194079, 16194081, 16079165.

Product
BD Pyxis Med 4000 Auxiliary (AUX), REF 314
Recalling firm
CareFusion 303, Inc.
Quantity
5 units
Distribution
Worldwide
Recall date
January 29, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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