Device recall
Z-2478-2026: Mito Red Light, Super Mobile
FDA device recall · Class II · MITO RED LIGHT INC
Key facts
| Recall number (Z-number) | Z-2478-2026 |
|---|---|
| Recall event | 98999 |
| Product | Mito Red Light, Super Mobile |
| Product code | ILY |
| Recalling firm | MITO RED LIGHT INC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015313684 |
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