PlainRecalls
FDA Devices Moderate Class II Ongoing

Diode Laser Hair Removal model: WLA-01

Reported: December 11, 2024 Initiated: August 23, 2024 #Z-0556-2025

Product Description

Diode Laser Hair Removal model: WLA-01

Reason for Recall

All model WLA-01 systems sold to US customers are found to have labeling non-compliances

Details

Distribution
Worldwide Distribution
Location
Beijing

Frequently Asked Questions

What product was recalled?
Diode Laser Hair Removal model: WLA-01. Recalled by WINGDERM ELECTRO-OPTICS LTD..
Why was this product recalled?
All model WLA-01 systems sold to US customers are found to have labeling non-compliances
Which agency issued this recall?
This recall was issued by the FDA Devices on December 11, 2024. Severity: Moderate. Recall number: Z-0556-2025.