# FDA recall Z-2477-2025

> **CareFusion 303, Inc.** · Class II · device recall initiated 2025-05-08.

## Product

BD Pyxis  Product Name / UDI-DI code / Catalog No.  BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303    BD Pyxis" MedStation" ES Tower / 10885403512674 / 352    BD Pyxis" Anesthesia Station ES / 10885403477836 / 327    BD Pyxis" MedStation" ES (Main) / 10885403512667 / 323    BD Pyxis" CII Safe ES / 10885403512605 / 1116-00    BD Pyxis" Enterprise Server / 10885403518348 and 10885403520341 / 1115-00    BD Pyxis" CIISafe, V9.X, SGL IM, BIO, / 10885403512520 / 111-221    BD Pyxis" CIISafe, V7.X, DBL INTG MAIN, BIO, SOLID DO / N/A / 111-194    BD Pyxis" MedBank Tower / 10885403512568 / 169-29    BD Pyxis" CIISafe, V8.X Desktop PC, Bio / N/A / 107-245-01    Supply Server / N/A / N/A    CCE Enterprise SW Site License (2-5) / N/A / N/A    BD Pyxis" Logistics / N/A / 806    BD Pyxis" SupplyStation" V9 / N/A / 317    Security Module / N/A / 139698-01    Supply itParActive RF V11 / N/A / 138566-01    BD Knowledge Portal for Medication Technologies / N/A / 136607-01    STOCKSTN V10.X WRD/W

## Reason for recall

Antivirus software was not consistently installed on impacted devices during the implementation process.

## Distribution

Worldwide - U.S 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, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. The countries of United Arab Emirates, Argentina, Australia, Belgium, Bahrain, Bermuda, Brazil, Bahamas, Canada, Switzerland, Germany, Egypt, Finland, France, United Kingdom, Hong Kong, Indonesia, Ireland, India, Italy, Jordan, Lebanon, Morocco, Mexico, Malaysia, New Zealand, Qatar, Saudi Arabia, Singapore, Thailand, Greece, Oman, and Taiwan.

## Key facts

- **Recall number:** Z-2477-2025
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-08
- **Report date:** 2025-09-03

- **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-2477-2025

## Citation

> AI Analytics. FDA recall Z-2477-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2477-2025. Source: US FDA. Licensed CC0.

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