MAX LUX CORP
MAX LUX CORP appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0246-2022, Class II) was initiated on October 26, 2021.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0246-2022 | Class II | The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular l | October 26, 2021 |