WINGDERM ELECTRO-OPTICS LTD.: Medical Device Recall in 2024 - (Recall #: Z-0556-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Diode Laser Hair Removal model: WLA-01

Product Classification:

Class II

Date Initiated: August 23, 2024

Date Posted: December 11, 2024

Recall Number: Z-0556-2025

Event ID: 95831

Reason for Recall:

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

Status: Ongoing

Product Quantity:

Code Information:

F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001

Distribution Pattern:

Worldwide Distribution

Voluntary or Mandated:

FDA Mandated