Recall archive / FDA device enforcement
Diode Laser Hair Removal model: WLA-01 — FDA record Z-0556-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 23, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Diode Laser Hair Removal model: WLA-01
- Reason
- All model WLA-01 systems sold to US customers are found to have labeling non-compliances
- Classification
- Class II
- Recalling firm
- WINGDERM ELECTRO-OPTICS LTD.
- Quantity
- Not supplied
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0556-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide Distribution
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Dec 11, 2024
- Recall initiation date
- Aug 23, 2024
- Center classification date
- Dec 5, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.