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U.S. Department of Health and Human Services

Medsun Reports
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Type of Device:
pump, infusion
Device Brand Name:
Alaris
Device Manufacturer's Name:
CareFusion 303, Inc.
Date of this Report:
(mm/dd/yyyy)
09/29/2015
Describe the Event
or Problem:
There have been 28 reported events, which were duplicated by clinical engineering where the "Air in Line" Sensor was not functioning on the Alaris Carefusion Pump, generating false alarms. The devices were sent to the manufacturer to replace the sensor.
the device(s) may have
caused or contributed to:
Potential for patient harm
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