CareFusion 303, Inc.: Medical Device Recall in 2024 - (Recall #: Z-2499-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9

Product Classification:

Class II

Date Initiated: June 24, 2024

Date Posted: August 14, 2024

Recall Number: Z-2499-2024

Event ID: 94947

Reason for Recall:

Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.

Status: Ongoing

Product Quantity: 12 units

Code Information:

UDI: 10885403512568/ Serial Number: 16073532 16068549 15940102 15815823 15854750 15422135 15879981 15639689 15935614 15937588 16083491 16087005

Distribution Pattern:

US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV.

Voluntary or Mandated:

Voluntary: Firm initiated