---
title: "Diode Laser Hair Removal model: WLA-01 — FDA record Z-0556-2025 | Is It on Recall"
description: "All model WLA-01 systems sold to US customers are found to have labeling non-compliances"
url: https://isitonrecall.com/recall/fda-device-z-0556-2025-diode-laser-hair-removal-model-wla-01/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Diode Laser Hair Removal model: WLA-01 — FDA record Z-0556-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 23, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Diode Laser Hair Removal model: WLA-01
- **Reason**: All model WLA-01 systems sold to US customers are found to have labeling non-compliances
- **Classification**: Class II
- **Recalling firm**: WINGDERM ELECTRO-OPTICS LTD.
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0556-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0556-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide Distribution

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Dec 11, 2024
- **Recall initiation date**: Aug 23, 2024
- **Center classification date**: Dec 5, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0556-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [WINGDERM ELECTRO-OPTICS LTD. records](https://isitonrecall.com/brand/wingderm-electro-optics-ltd/)