Device recall
Z-0526-2013: EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation
FDA device recall · Class II · EEG Info
Key facts
| Recall number (Z-number) | Z-0526-2013 |
|---|---|
| Recall event | 63824 |
| Product | EEG NeuroAmp, Model Number: CS 10090; CS 10137. Biofeedback and Relaxation |
| Product code | HCC |
| Recalling firm | EEG Info |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2013 |
| 510(k) numbers | K073557 |
| FEI number | 3009138210 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database