Reported Jan 25, 2017 · Terminated
Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a…
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?
3 of 3 products
| Model / number | Product as published |
|---|---|
8100 | and AIL sensor kits |
147083-102 | and |
49000221. | 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
- All products manufactured or serviced in the time period October 2011 through June 2015.
- Amount recalled
- 382,635 units
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.
Using this product could cause serious injury, illness or death — stop using it now.
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