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

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

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

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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.

. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.


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