Device recall
Z-1807-2026: The product is a handheld ultraviolet-C germicidal wand and contains two…
FDA device recall · Class II · Uvlizer c/o RAIS INTERNATIONAL LLC
Key facts
| Recall number (Z-number) | Z-1807-2026 |
|---|---|
| Recall event | 98747 |
| Product | The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 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