Carefusion Provides Update on Voluntary Recall of Neurilogical Monitoring Software and Devices
January 21, 2012 | Food and Drug, Recalls
CareFusion issued the following update regarding its voluntary recall of the Nicolet® Cortical Stimulator Control Unit, Nicolet® C64 Stimulus Switching Unit (SSU) Amplifier and NicoletOne Software with Cortical Stimulator License. The FDA has classified this action as a Class I recall.
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