Recall: Alaris Infusion Pump

The FDA has announced a Class I recall of version 9.1.18 of the software in the Alaris Infusion Pump model 8100 made by CareFusion 303, Inc, because the “delay until” and “multidose” options may malfunction.  For details see http://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm398178.htm.  Class I recalls are used when serious injury or death may result.

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