# FDA recall Z-0906-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2023-04-05.

## Product

BD Pyxis MedStation  ES (Med ES Main), REF: 323; and BD Pyxis MedStation  ES (Med ES Main Tower), REF: 352

## Reason for recall

Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.

## Distribution

US Nationwide distribution in the states of NY, NC, LA.

## Key facts

- **Recall number:** Z-0906-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-05
- **Report date:** 2025-01-22

- **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-0906-2025

## Citation

> AI Analytics. FDA recall Z-0906-2025. Retrieved 2026-08-19 from https://api.ai-analytics.org/recall/Z-0906-2025. Source: US FDA. Licensed CC0.

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