CareFusion 303, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0093-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

BD Pyxis CII Safe ES, REF: 1116-00; and BD Pyxis : CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01; CII Safe ES Desktop PC, W-LESS SCNR, BIO, REF: 107-255-01; Enterprise Server, REF: 1115-00, 134157-01, 137670-02, 134148-01, 135292-01, 136449-01, 133760-01

Product Classification:

Class II

Date Initiated: September 6, 2023

Date Posted: October 18, 2023

Recall Number: Z-0093-2024

Event ID: 93016

Reason for Recall:

When global edit is used to update multiple formulary properties simultaneously, the following properties: 1) Require Lot Number on Recall, 2) Access Destruction Bin (Witness), 3) Add to Destruction Bin (Count/Empty), 4) CII Safe Stock Out Notice are, without user warning, overwritten to the value NO , which could result in diversion of controlled substances from the automated dispensing cabinet.

Status: Ongoing

Product Quantity: 61

Code Information:

REF: 1116-00, UDI-DI: 10885403512605. Software Versions: 1.7.3 and 1.7.4 (Limited commercial release)

Distribution Pattern:

US Nationwide distribution in the states of LA, NC, NY, MI, MA, NV, KS, IA, CA.

Voluntary or Mandated:

Voluntary: Firm initiated