Class II

Medical Device Recall: Diode Laser Hair Removal model: WLA-01

WINGDERM ELECTRO-OPTICS LTD. · August 23, 2024

Reason for Recall

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

Distribution

Worldwide Distribution

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0556-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

WINGDERM ELECTRO-OPTICS LTD. Medical Device Recall: Diode Laser Hair Removal model: WLA-01 | SafeCheck