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

Recall Z-2489-2024 — BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9

U.S. FDA — Device Enforcement · United States · 2024-06-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2489-2024
Date of alert
2024-06-24
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 software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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