Drug recall
EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation
FDA recall event 63824 · Class II · EEG Info
Key facts
| Event ID | 63824 |
|---|---|
| Recall numbers | Z-0526-2013 |
| Recalling firm | EEG Info |
| Product type | Devices |
| Products | EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Nov 15, 2012 |
| Report date | Dec 26, 2012 |
| Termination date | Jun 11, 2013 |
| City | Woodland Hills |
| State | CA |
| Country | United States |
| FEI number | 3009138210 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: