# FDA recall Z-1124-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2024-02-23.

## Product

BD Pyxis MedStation Auxiliary 4000 REF: 306.  Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

## Reason for recall

Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet   which could result in delay in accessing medications.

## Distribution

US: Nationwide  OUS:JP	IT	IN	DE	GB	KR	NL	TW	ES	BE	AU	BH	CA	BR	NZ	FR	AR	QA	MX	CL	TR	SA	MY	CH	IL	IE	TH	SG	KW	MA	FI	AE	EG	BS	BM	GR	MC	PL	LB	MO	IQ	TN	NO	PH	CN	HK	CO	JO	OM

## Key facts

- **Recall number:** Z-1124-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-23
- **Report date:** 2025-02-19

- **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-1124-2025

## Citation

> AI Analytics. FDA recall Z-1124-2025. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1124-2025. Source: US FDA. Licensed CC0.

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