Reported May 21, 2014 · Terminated

Alaris Pump model 8100 with software version 9.1.18 and software upgrade kits with "Delay Until" Option and "Multidose"…

CareFusion 303, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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?

  • Alaris Pump model 8100 with software version 9.1.18 and software upgrade kits with "Delay Until" Option and "Multidose" Feature The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural.
Lot codes and dates
  • Serial no.

    3,269 of 3,269 codes

    • 14031885
    • 14031892
    • 14031897
    • 14031916
    • 14032037
    • 14032060
    • 14032075
    • 14032083
    • 14032091
    • 14032105
    • 14032510
    • 14032588
    • 14032682
    • 14032683
    • 14032684
    • 14032686
    • 14032729
    • 14032741
    • 14032774
    • 14032775
    • 14035370
    • 14035776
    • 14035827
    • 14035855
    • 14035963
    • 14036178
    • 14036191
    • 14036215
    • 14036219
    • 14036422
    • 12773501
    • 13184780
    • 13932274
    • 13932283
    • 13932301
    • 13932329
    • 13932333
    • 13990520
    • 13990521
    • 13990661
    • 13990694
    • 13990697
    • 13990698
    • 13990699
    • 13990701
    • 13990738
    • 13990741
    • 13990742
    • 13990807
    • 13990872
    • 13990928
    • 13990930
    • 13990938
    • 13990955
    • 13990957
    • 13990958
    • 13990976
    • 13990978
    • 13990982
    • 13990985
Amount recalled
57,219 units total (55,756 units in US)

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it may have a software issue that results in situation where the pump module will not properly delay an infusion when the "Delay Until" option or "Multidose" feature is used.

Using this product could cause serious injury, illness or death — stop using it now.

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

Notice updated Mar 1, 2017 · Data as of Sep 19, 6:16 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.