# FDA recall Z-0975-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2023-02-14.

## Product

BD Pyxis Med ES Auxiliary (AUX), REF 343

## Reason for recall

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified:    Situation 1: Door Latch Failure,   Situation 2: Cable Ribbon Damage,   Situation 3: Magnet Falling Out,

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-0975-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-14
- **Report date:** 2025-01-29

- **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-0975-2025

## Citation

> AI Analytics. FDA recall Z-0975-2025. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0975-2025. Source: US FDA. Licensed CC0.

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