FDA Device recall Z-2477-2025
BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis" MedStation" ES Tower / 1…
- FDA Device
- Class II
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class II recall of BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis" MedStation" ES Tower / 1… by Carefusion 303, citing antivirus software was not consistently installed on impacted devices during the implementation process.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2477-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-08 |
| Published | 2025-09-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
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.
Reason
Antivirus software was not consistently installed on impacted devices during the implementation process.
Identifiers
| code_info | BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 Atlas Key / Co…BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 Atlas Key / Computer Name: DF36449C-9896-4A27-BC18-481981535F84 OR2 993BA58F-B5FB-49E8-AE94-BC81E0A93C2A ER-PED FF9AD713-320E-4317-94C0-1A7F57F1AA63 K3 25845A1C-20A3-44BA-8D78-9C9DC001F5B8 PYXH5SASC 2BFA94A6-6192-4ACA-B495-06BA07DC2D73 ESC-WARD1 38404D6B-8356-476A-970F-E4F9CE5731DB WC A9EF86BC-6DF5-4F7F-AE54-6F51773D343E THEATRE12W 1B194D06-1F1A-4930-AA42-57BBDF1E72EE OAKTON B7F75FB9-7480-4C2F-8E91-66D5AF2C0607 MEDSURG 390D8BC7-36E3-4D8D-8CB6-E9360C197DE5 W15 D83C62B5-8D53-4A6B-85AD-E0119DF3E186 THEATRE6 63605AE3-DC21-45BB-A882-F40E22EF811E MEDSHIP 1D2BA923-E0B0-4DE4-BFDB-69247B773273 ED-1 4D0B213F-D42B-4829-9431-1C4D482B1D67 THEATRE 3482ADD7-D610-4FD7-B561-2CC85D4028D4 4K102713S1 214209FD-6AD2-48CE-A15F-8252209D60EF HAMPDENFC_pyx 0B8D0E14-7E8E-4AE7-B492-726887F4411C W5-AUX CF5045AE-86EE-4698-ACEA-3581C9EC7CD1 THEATRE7 92F5A739-E0CA-4C9B-AD3D-27CF3921F944 ACARE 00AAEB97-9E1B-4738-B7 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2477-2025%22
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