FDAFDA · Food and drugs·Recall number Z-0556-2025
Diode Laser Hair Removal model: WLA-01
Published December 11, 2024 · Recall initiated: August 23, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
All model WLA-01 systems sold to US customers are found to have labeling non-compliances
What to do
FDA Mandated · Letter
Recall details
- Manufacturer
- WINGDERM ELECTRO-OPTICS LTD.
- Distributor
- Worldwide Distribution
- Lot
- F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- China
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