# FDA recall Z-1120-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-01-08.

## Product

(1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis  MedStation 4000 Console,  Catalog No. 309; (5) BD Pyxis  MedStation 4000,  Catalog No. 303; (6) BD Pyxis  Anesthesia System 4000, Catalog No. 338

## Reason for recall

Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation.

## Distribution

Domestic distribution nationwide US. International distribution to North America, Latin America, EMEA, and Greater Asia.

## Key facts

- **Recall number:** Z-1120-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-08
- **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-1120-2025

## Citation

> AI Analytics. FDA recall Z-1120-2025. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-1120-2025. Source: US FDA. Licensed CC0.

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