Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2017-2025 — Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], 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

U.S. FDA — Device Enforcement · United States · 2025-05-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2017-2025
Date of alert
2025-05-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403512629
Reported risk: During automated dispensing cabinet upgrade/installation/reimaging, component manager was left in installed mode, and if a Microsoft patch is then installed this may lead to an error preventing user access to the dispensing software application, which may lead to delay in access to medications/supplies, and delivery/replenishment of patient specific orders; which may lead to delay in patient care.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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