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

Recall Z-1545-2025 — BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated dispensing cabinets (ADC) intended to securely store and dispense medications to a qualified and authorized user in a clinical settings.

U.S. FDA — Device Enforcement · United States · 2025-03-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1545-2025
Date of alert
2025-03-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403512568
Reported risk: Due to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This bug can also result in the CUBIE opening more times than needed for the transaction to be completed, which may result in a patient receiving more than the intended dose of medication.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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