Device recall
Z-0972-2024: NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product…
FDA device recall · Class II · THOR Photomedicine Ltd
Key facts
| Recall number (Z-number) | Z-0972-2024 |
|---|---|
| Recall event | 93723 |
| Product | NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL |
| Product code | ILY |
| Recalling firm | THOR Photomedicine Ltd |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003899624 |
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