Official recall record

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation 4000 Main 10885403512

US FDA — Medical Devices · 2025-05-08 · United StatesClass II

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2025-05-08
Country of alert: United States
Alert level: Class II
Alert type: recall
Barcode (EAN/GTIN): 10885403512629
Brand on record: CareFusion 303, Inc.
Product category: Medical Device

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

Same barcode in other registries

The same EAN appears in 4 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

2024-04-15 · US FDA — Medical Devices
BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
2023-02-14 · US FDA — Medical Devices
BD Pyxis MedStation 4000 Main, REF 303
2024-02-23 · US FDA — Medical Devices
BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized he
2026-04-30 · US FDA — Medical Devices
BD Pyxis MedStation 4000 REF: 303 Medication cabinet

Other recalls from this brand

All 11 official recall notices naming CareFusion 303, Inc. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.