# FDA recall Z-0928-2023

> **CareFusion 303, Inc.** · Class II · device recall initiated 2022-12-12.

## Product

BD Pyxis MedBank System - Product Label/labeling pending

## Reason for recall

Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.

## Distribution

U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, WA, WI, and WV.

## Key facts

- **Recall number:** Z-0928-2023
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-12
- **Report date:** 2023-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0928-2023

## Citation

> AI Analytics. FDA recall Z-0928-2023. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-0928-2023. Source: US FDA. Licensed CC0.

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