Device recall
Z-0082-2024: CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator…
FDA device recall · Class II · RoyalVibe Health Ltd.
Key facts
| Recall number (Z-number) | Z-0082-2024 |
|---|---|
| Recall event | 92789 |
| Product | CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe Therapy Balls |
| Product code | OHV |
| Recalling firm | RoyalVibe Health Ltd. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3022074304 |
At a glance
- None 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