MAX LUX CORP Recall 89050
Description: 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.
MAX LUX CORP Recall 89050 Information
| Status | Ongoing |
| Mandated? | FDA Mandated |
| Recall Number | Z-0246-2022 |
| Event ID | 89050 |
| Event Description | 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 Type | Devices |
| Distribution | US Nationwide Distribution |
| Quantity | 9900 units |
| Recall Reason | Excessive ultraviolet-C radiation |
| Device Classification | 20211208 |
| Device Code Info | Safe-T Lite |
| Center Classification Date | 20211129 |
| Recall Initiation Date | 20211026 |
| Recalling Firm | MAX LUX CORP |
| Initial Notification | Letter |
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