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
140318851403189214031897140319161403203714032060140320751403208314032091140321051403251014032588140326821403268314032684140326861403272914032741140327741403277514035370140357761403582714035855140359631403617814036191140362151403621914036422127735011318478013932274139322831393230113932329139323331399052013990521139906611399069413990697139906981399069913990701139907381399074113990742139908071399087213990928139909301399093813990955139909571399095813990976139909781399098213990985
- Serial no.
- 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.
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