Reported Dec 18, 2024 · Ongoing

BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324

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 7 Drawer Auxiliary Tower
  • REF324
Lot codes and dates
  • All software versions
  • REF/UDI-DI

    3,548 of 3,548 codes

    • 324/10885403512681/
    • 12440840
    • 12440841
    • 12448208
    • 12452252
    • 12452264
    • 12455476
    • 12462734
    • 12462735
    • 12463676
    • 12468609
    • 12468612
    • 12468607
    • 12468608
    • 12468610
    • 12468671
    • 12468672
    • 12468674
    • 12468670
    • 12468673
    • 12468611
    • 12474015
    • 12474022
    • 12473810
    • 12473813
    • 12473815
    • 12473816
    • 12473817
    • 12473811
    • 12473921
    • 12474012
    • 12474071
    • 12474014
    • 12473887
    • 12473922
    • 12474013
    • 12473807
    • 12473812
    • 12473808
    • 12473809
    • 12476548
    • 12495456
    • 12499285
    • 12502858
    • 12502857
    • 12503069
    • 12508589
    • 12508584
    • 12508578
    • 12508579
    • 12508587
    • 12508580
    • 12510555
    • 12510559
    • 12510393
    • 12520264
    • 12520266
    • 12520267
    • 12520269
    • 12528519
Amount recalled
40,763

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.

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

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 6:18 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.