Reported Jan 29, 2025 · Ongoing

BD Pyxis MedStation 4000 Main, REF 303

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 4000 Main
    • REF 303
Lot codes and dates
  • UDI/DI 10885403512629
  • Serial Numbers

    3,256 of 3,256 codes

    • 12439536
    • 12439538
    • 12439539
    • 12439540
    • 12439541
    • 12439544
    • 12440786
    • 12440787
    • 12440788
    • 12440789
    • 12440790
    • 12440791
    • 12440792
    • 12440978
    • 12440979
    • 12441431
    • 12443165
    • 12446066
    • 12448071
    • 12448072
    • 12448073
    • 12448074
    • 12448142
    • 12450907
    • 12450908
    • 12450909
    • 12450910
    • 12450911
    • 12450912
    • 12450913
    • 12450914
    • 12450915
    • 12450968
    • 12450970
    • 12450971
    • 12450973
    • 12450974
    • 12450975
    • 12450976
    • 12451251
    • 12451628
    • 12452651
    • 12452991
    • 12452993
    • 12453011
    • 12453012
    • 12453013
    • 12455427
    • 12455859
    • 12457587
    • 12457588
    • 12457589
    • 12457590
    • 12459775
    • 12461364
    • 12461365
    • 12461368
    • 12461369
    • 12461516
    • 12461517
Amount recalled
13055 units

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Why it was recalled

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

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

Want the full recall guide?

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, 4:56 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.