# FDA recall Z-2500-2024

> **CareFusion 303, Inc.** · Class II · device recall initiated 2024-06-24.

## Product

BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9

## 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.

## Distribution

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.

## Key facts

- **Recall number:** Z-2500-2024
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-24
- **Report date:** 2024-08-14

- **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-2500-2024

## Citation

> AI Analytics. FDA recall Z-2500-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2500-2024. Source: US FDA. Licensed CC0.

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