WINGDERM ELECTRO-OPTICS LTD. recalls Diode Laser Hair Removal model: WLA-01
- Recall date
- August 23, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0556-2025
- FDA classification
- Class II
- Brand / firm
- WINGDERM ELECTRO-OPTICS LTD.
- Sold / distributed
- Worldwide Distribution
Why it was recalled
All model WLA-01 systems sold to US customers are found to have labeling non-compliances
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Diode Laser Hair Removal model: WLA-01
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