CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1119-2025)

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:

(1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis CII Safe ES, Catalog No. 1116-00

Product Classification:

Class II

Date Initiated: January 8, 2025

Date Posted: February 19, 2025

Recall Number: Z-1119-2025

Event ID: 96055

Reason for Recall:

Software issues could potentially result in: 1) delays in accessing dispensing software application, 2) wrong therapy (dose, item, timing, etc.), or 3) unauthorized access and/or compliance related issues

Status: Ongoing

Product Quantity: 137,741 total

Code Information:

(1) Pyxis MedStation ES, Catalog No. 323, UDI-DI 10885403512667; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327, UDI-DI 10885403477836; (3) Pyxis MedStation ES Tower, Catalog No. 352, UDI-DI 10885403512674; (4) BD Pyxis CII Safe ES, Catalog No. 1116-00, UDI-DI 10885403512605; All Serial Numbers; Software Versions v1.10 and prior Affected

Distribution Pattern:

Domestic distribution nationwide. International distribution to North America, Latin America, EMEA, and Greater Asia.

Voluntary or Mandated:

Voluntary: Firm initiated