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

Recall Z-1050-2025 — BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and Pyxis" MedStation 4000 are automated dispensing cabinets (ADC) that are intended to securely store and dispense medications to a qualified and authorized healthcare provider.

U.S. FDA — Device Enforcement · United States · 2023-02-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1050-2025
Date of alert
2023-02-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403512698
Reported risk: Due to an increase in complaints of door latch assembly failures that may cause the doors to be left in an open state potentially causing inventory discrepancies, a delay in access to medication and/or diversion of medication.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.