FDAClass IIDecember 26, 2012

EEG NeuroAmp recall: Labeling Error

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

Why was EEG NeuroAmp recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial Number: 0001-3343.

Product
EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation
Recalling firm
EEG Info
Quantity
1308 units
Distribution
Nationwide Distribution
Recall date
December 26, 2012
Classification
Class II
Status
Terminated
Agency
FDA (device)
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