Device recall
Z-0246-2022: The product is a handheld ultraviolet-C germicidal wand and contains two…
FDA device recall · Class II · MAX LUX CORP
Key facts
| Recall number (Z-number) | Z-0246-2022 |
|---|---|
| Recall event | 89050 |
| Product | The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces. |
| Product code | RHP |
| Recalling firm | MAX LUX CORP |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3017032819 |
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