CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1125-2025)

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 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

Product Classification:

Class II

Date Initiated: February 23, 2024

Date Posted: February 19, 2025

Recall Number: Z-1125-2025

Event ID: 96041

Reason for Recall:

Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.

Status: Ongoing

Product Quantity:

Code Information:

UDI: 10885403512629/ Serial Numbers: 16153360 16161369 16161370 16161371 16187328 16187329 16187330 15495060 15930189 16161368 16173444 16283947

Distribution Pattern:

US: Nationwide OUS:JP IT IN DE GB KR NL TW ES BE AU BH CA BR NZ FR AR QA MX CL TR SA MY CH IL IE TH SG KW MA FI AE EG BS BM GR MC PL LB MO IQ TN NO PH CN HK CO JO OM

Voluntary or Mandated:

Voluntary: Firm initiated