FDA Alerts

Class I Recall: CareFusion NicoletOne Software Used with CareFusion Cortical Stimulator Control Unit

CareFusion is recalling these affected devices and software for two reasons: The device’s software incorrectly indicates stimulation is delivered to a different electrode than the one selected A short circuit may develop

Wed Oct 05 2011By Other Author

CareFusion is recalling these affected devices and software for two reasons:

  • The device’s software incorrectly indicates stimulation is delivered to a different electrode than the one selected
  • A short circuit may develop between the cortical stimulator control unit and the stimulus switching unit amplifier
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