CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1120-2025)

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) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis MedStation 4000 Console, Catalog No. 309; (5) BD Pyxis MedStation 4000, Catalog No. 303; (6) BD Pyxis Anesthesia System 4000, Catalog No. 338

Product Classification:

Class II

Date Initiated: January 8, 2025

Date Posted: February 19, 2025

Recall Number: Z-1120-2025

Event ID: 96056

Reason for Recall:

Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation.

Status: Ongoing

Product Quantity: 193067

Code Information:

(1)BD Pyxis MedStation ES, Catalog No. 323, UDI-DI 10885403512667; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327, UDI-DI 10885403477836; (3) BD Pyxis MedStation ES Tower, Catalog No. 352, UDI-DI 10885403512674; ALL serial numbers; software versions v1.10 and prior. (4) BD Pyxis MedStation 4000 Console, Catalog No. 309, All serial numbers and all software versions, UDI-DI: 10885403512636; (5) BD Pyxis MedStation 4000, Catalog No. 303, All serial numbers and all software versions, UDI-DI: 10885403512629 (HW), 10885403513787 (SW); (6) BD Pyxis Anesthesia System 4000, Catalog No. 338, All serial numbers and all software versions, UDI-DI: 10885403477829 (HW), 10885403513787 (SW)

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated