Reported Feb 5, 2025 · Ongoing

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and…

CareFusion 303, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386

Is this the product you have?

  • 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.
Lot codes and dates
  • BD Pyxis
  • MedStation ES AUX Tower Catalog Number343
  • UDI-DI code10885403512698
  • Serial Number/Equipment Number

    3,605 of 3,605 codes

    • 14535900
    • 14535900
    • 14535901
    • 14535901
    • 14535902
    • 14535902
    • 14535903
    • 14535903
    • 14535904
    • 14535904
    • 14535905
    • 14535905
    • 14535906
    • 14535906
    • 14535907
    • 14535907
    • 14535908
    • 14535908
    • 14535910
    • 14535910
    • 14535912
    • 14535912
    • 14535913
    • 14535913
    • 14535916
    • 14535916
    • 14535919
    • 14535919
    • 14535922
    • 14535922
    • 14535924
    • 14535924
    • 14535926
    • 14535926
    • 14535928
    • 14535928
    • 14535930
    • 14535930
    • 14535932
    • 14535932
    • 14535934
    • 14535934
    • 14535936
    • 14535936
    • 14535937
    • 14535937
    • 14535939
    • 14535939
    • 14535941
    • 14535941
    • 14535943
    • 14535943
    • 14535945
    • 14535945
    • 14535947
    • 14535947
    • 14535949
    • 14535949
    • 14535951
    • 14535951
Amount recalled
Initial: 27,666 Expansion: 5,923 = 33,589 systems

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:56 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.