FDA Device recall Z-0556-2025
Diode Laser Hair Removal model: WLA-01
- FDA Device
- Class II
- ongoing
- Published 2024-12-11
On 2024-12-11 the FDA classified a Class II recall of Diode Laser Hair Removal model: WLA-01 by Wingderm Electro Optics, citing all model WLA-01 systems sold to US customers are found to have labeling non-compliances.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0556-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-08-23 |
| Published | 2024-12-11 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Wingderm Electro Optics |
| Distribution | n/a |
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
Identifiers
| code_info | F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0556-2025%22
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