FDA Recall: Antivirus software was not consistently installed

Company: CareFusion 303, Inc.
Date of Enforcement Report: 8/28/2025
Class: II

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/WL SCANNERS / N/A / 132-53-02 PRS STOCKSTN V10.X WRD/WL SCANNERS / N/A / 132-53-01 STOCKSTN V10.X WIRED SCANNER / N/A / 132-52-02 PRS STOCKSTN V10.X WIRED SCANNER / N/A / 132-52-01 BD Pyxis” CII Safe ES, Desktop PC / N/A / 1156-00 BD Pyxis” SupplyStation” Panel PC V11 / N/A / 1132-00 Pyxis” SupplyRoller V11 / N/A / 1127-00 Dell 640 Server / N/A / 1128-00 BD Pyxis” SupplyStation” System V11 / N/A / 1123-00 BD Pyxis” SupplyRoller V10 / N/A / 1101-00 BD Pyxis” SupplyStation” System V10 / **** / 347 BD Pyxis CII Safe,V9.X DESKTOP PC / **** / 107-252-01 BD Pyxis CII Safe,V7.X,DBL INTG MAIN,BIO,CLEAR DO 111-191 BD Pyxis CII Safe, V9.X, DBL IM, BIO, SLD DOORS / **** / 111-215 BD Care Coordination Engine (CCE) / **** / 134056-01 The Pyxis devices are automated medication dispensing cabinet that is intended to securely store and dispense medications to a qualified and authorized healthcare provider.

Recall Number:

Z-2477-2025

REASON:

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

RECALLING FIRM/MANUFACTURER:

CareFusion 303, Inc

VOLUME:

8353 devices (6738 U.S. and 1615 O.U.S.)

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.

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.