PlainRecalls
FDA Devices Moderate Class II Ongoing

BD Pyxis Med ES Auxiliary (AUX), REF 343

Reported: January 29, 2025 Initiated: February 14, 2023 #Z-0975-2025

Product Description

BD Pyxis Med ES Auxiliary (AUX), REF 343

Reason for Recall

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,

Details

Recalling Firm
CareFusion 303, Inc.
Units Affected
5918 units
Distribution
Worldwide
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
BD Pyxis Med ES Auxiliary (AUX), REF 343. Recalled by CareFusion 303, Inc.. Units affected: 5918 units.
Why was this product 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,
Which agency issued this recall?
This recall was issued by the FDA Devices on January 29, 2025. Severity: Moderate. Recall number: Z-0975-2025.