EEG Info: Medical Device Recall in 2012 - (Recall #: Z-0526-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 15, 2012

Date Posted: December 26, 2012

Recall Number: Z-0526-2013

Event ID: 63824

Reason for Recall:

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

Status: Terminated

Product Quantity: 1308 units

Code Information:

Serial Number: 0001-3343.

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated