CareFusion 303, Inc.: Medical Device Recall in 2024 - (Recall #: Z-2503-2024)

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-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9

Product Classification:

Class II

Date Initiated: June 24, 2024

Date Posted: August 14, 2024

Recall Number: Z-2503-2024

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: 16 units

Code Information:

UDI: 10885403512568/ Serial Number: 16210468 16274000 16232272 16209954 16209953 16097230 16184767 16101319 16095341 16112043 15815836 15631124 15632972 15937573 16073534 16173241

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