Device recall
Z-1942-2024: WAVi Research EEG Desktop System is comprised of the WAVi Research EEG Desktop…
FDA device recall · Class II · WAVi Co.
Key facts
| Recall number (Z-number) | Z-1942-2024 |
|---|---|
| Recall event | 94498 |
| Product | WAVi Research EEG Desktop System is comprised of the WAVi Research EEG Desktop Software with Instruction Manual and Brochure, and Heart Rate Variability (HRV) Ear Clips. The system kit also incorporates use of the firm's cleared EEG analysis technology (the WAVi SCAN EEG System and Accessories, and… |
| Product code | GWQ |
| Recalling firm | WAVi Co. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3013757456 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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