CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0976-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

BD Pyxis Med 4000 Auxiliary (AUX), REF 314

Product Classification:

Class II

Date Initiated: February 14, 2023

Date Posted: January 29, 2025

Recall Number: Z-0976-2025

Event ID: 96053

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,

Status: Ongoing

Product Quantity: 5 units

Code Information:

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

Distribution Pattern:

Worldwide

Voluntary or Mandated:

Voluntary: Firm initiated