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FDAFDA · Food and drugs·Recall number Z-0526-2013

EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation

Published December 26, 2012 · Recall initiated: November 15, 2012

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

EEG Info, Inc. is recalling the EEG Neuroamp device because they have identified a potential risk associated with the mislabeling of certain devices.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
EEG Info
Distributor
Nationwide Distribution
Lot
Serial Number: 0001-3343.
Risk classification
Class II
Area (FDA)
device
Country
United States

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