CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0906-2025)

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 MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352

Product Classification:

Class II

Date Initiated: April 5, 2023

Date Posted: January 22, 2025

Recall Number: Z-0906-2025

Event ID: 96002

Reason for Recall:

Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.

Status: Ongoing

Product Quantity: 622

Code Information:

Software v1.7.3. REF/UDI-DI: 323/10885403512667, 352/10885403512674

Distribution Pattern:

US Nationwide distribution in the states of NY, NC, LA.

Voluntary or Mandated:

Voluntary: Firm initiated