# FDA recall Z-1932-2024

> **CareFusion 303, Inc.** · Class II · device recall initiated 2024-04-15.

## Product

BD Pyxis(TM) Anesthesia Station 4000,  REF: 338

## Reason for recall

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

## Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, 	CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, 	ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of South Africa, Kuwait, Qatar, Singapore, Bermuda, United Arab Emirates, Argentina, Australia, Belgium, Bahrain, Brazil, Bahamas, Canada, Chile, China, Germany, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Italy, Japan,  South Korea, Lebanon, Morocco, Mexico, New Zealand, Oman, Portugal, Thailand, Taiwan.

## Key facts

- **Recall number:** Z-1932-2024
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-15
- **Report date:** 2024-06-05

- **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-1932-2024

## Citation

> AI Analytics. FDA recall Z-1932-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1932-2024. Source: US FDA. Licensed CC0.

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