Carefusion Provides Update on Voluntary Recall of Neurilogical Monitoring Software and Devices

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Carefusion Provides Update on Voluntary Recall of Neurilogical Monitoring Software and Devices

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Carefusion Provides Update on Voluntary Recall of Neurilogical Monitoring Software and Devices

01/20/2012 12:16 PM EST

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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