Reported Dec 11, 2024 · Ongoing
Diode Laser Hair Removal model: WLA-01
Wingderm Electro-Optics Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: WINGDERM ELECTRO-OPTICS LTD. · Room 312 · Beijing · N/A
Is this the product you have?
- Diode Laser Hair Removal modelWLA-01
- Lot codes and dates
- F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
All model WLA-01 systems sold to US customers are found to have labeling non-compliances
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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