Reported Jul 19, 2017 · Terminated
Alaris Pump Module model 8100
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?
- Alaris Pump Module model 8100
- Lot codes and dates
- Notification will be distributed to all Alaris Pumps customers with pumps manufactured between June 2002 through June 2004.
- Amount recalled
- 35,940 units
Why it was recalled
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
This product could cause temporary or reversible health problems — stop using it.
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