Reported Jan 18, 2023 · Ongoing

BD Pyxis MedBank System - Product Label/labeling pending

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 MedBank System - Product Label/labeling pending
Lot codes and dates
  • BD Pyxis"
  • MedBank Tower Main UDI Code10885403512568
  • Catalog Numbers
    • 169-23 to 169-81
    • 169-100
    • 169-132
    • 169-138
    • 169-139 BD Pyxis"
  • MedBank Mini Main UDI Code10885403512544
  • Catalog Numbers169-101 - 169-113, 169-137 BD Pyxis" MEDFLEX BD Pyxis" MEDFLEX 2.0
  • UDI Codes10885403512704
  • Catalog Numbers1119-00 1139-00
  • MedBank 200/500 UDI CodeN/A
  • Catalog Numbers1137-00 BD Pyxis MEDPASS v1.0
  • or prior UDI Code10885403513817
  • Catalog NumberNot Provided BD Pyxis" MedBank Cabinet Software v2.2
  • or prior UDI Codes10885403513794
  • Catalog NumberN/A
  • Affected Serial Numbers

    3,557 of 3,557 codes

    • 12940473
    • 12971999
    • 12972001
    • 12972004
    • 12972006
    • 12972007
    • 12982486
    • 12982487
    • 12982488
    • 12982489
    • 12982490
    • 12982491
    • 12982492
    • 12982493
    • 13517006
    • 13523350
    • 13598718
    • 13629024
    • 13727050
    • 13739164
    • 13754724
    • 13766710
    • 13766711
    • 13767953
    • 13769979
    • 13770265
    • 13770291
    • 13789575
    • 13792769
    • 13801727
    • 13802400
    • 13817034
    • 13819501
    • 13826187
    • 13829362
    • 13829363
    • 13829364
    • 13832440
    • 13843251
    • 13849951
    • 13853916
    • 13853918
    • 13856246
    • 13873024
    • 13875126
    • 13875127
    • 13877499
    • 13877712
    • 13877713
    • 13877714
    • 13877715
    • 13879543
    • 13879544
    • 13880558
    • 13883357
    • 13884040
    • 13884382
    • 13884848
    • 13884851
    • 13885104
    15
Amount recalled
6,796 systems

Where it was sold

Why it was recalled

Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.

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, 7:47 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.