Reported Dec 18, 2024 · Ongoing

BD Pyxis CII Safe ES, REF: 1116-00

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 CII Safe ES
  • REF1116-00
Lot codes and dates
  • All software versions
  • REF/UDI-DI

    219 of 219 codes

    • 1116-00/10885403512605/
    • 15938609
    • 15938608
    • 15960426
    • 15977244
    • 15977243
    • 15997587
    • 15997584
    • 15997586
    • 16001276
    • 16004167
    • 16004170
    • 16004168
    • 16006959
    • 16016028
    • 16018286
    • 16018285
    • 16027068
    • 16034363
    • 16038606
    • 16038608
    • 16042040
    • 16043100
    • 16051041
    • 16052300
    • 16056892
    • 16081629
    • 16089006
    • 16107354
    • 16121844
    • 16124176
    • 16124177
    • 16124175
    • 16124174
    • 16124178
    • 16142019
    • 16142717
    • 16147368
    • 16150604
    • 16150317
    • 16154380
    • 16154381
    • 16179910
    • 16185906
    • 16186402
    • 16186403
    • 16188916
    • 16188917
    • 16189876
    • 16191858
    • 16191855
    • 16192478
    • 16192476
    • 16198735
    • 16205805
    • 16205708
    • 16210899
    • 16211121
    • 16211303
    • 16211474
Amount recalled
218

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, 7:33 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.