FDAClass IIJune 10, 2026

BD Pyxis Anesthesia Station 4000 recall

BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet

Why was BD Pyxis Anesthesia Station 4000 recalled?

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

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?

All Serial Numbers/UDI:10885403477829

Product
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Recalling firm
CareFusion 303, Inc.
Quantity
1 unit
Distribution
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Recall date
June 10, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls