Device recall
Z-1808-2026: The product is a handheld ultraviolet-C germicidal wand and contains a…
FDA device recall · Class II · Uvlizer c/o RAIS INTERNATIONAL LLC
Key facts
| Recall number (Z-number) | Z-1808-2026 |
|---|---|
| Recall event | 98742 |
| Product | The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two peak emission wavelengths at 274 nm and 397 nm. |
| Product code | RHP |
| Recalling firm | Uvlizer c/o RAIS INTERNATIONAL LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3031733296 |
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