Drug recall
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with…
FDA recall event 89050 · Class II · MAX LUX CORP
Key facts
| Event ID | 89050 |
|---|---|
| Recall numbers | Z-0246-2022 |
| Recalling firm | MAX LUX CORP |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA Requested |
| Reason for recall | Excessive ultraviolet-C radiation |
| Initiation date | Oct 26, 2021 |
| Report date | Dec 8, 2021 |
| City | Yangjiangyangjiang |
| Country | China |
| FEI number | 3017032819 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: