Wingderm Electro Optics recalls
Wingderm Electro Optics appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2024-12-11.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 2 |
|---|---|
| Published | 2024-12-11 |
| By agency | FDA Device (2) |
| By classification | Class II (2) |
| By status | ongoing (2) |
Recalls
- Diode Laser Hair Removal model: WLA-01
FDA Device · Class II · 2024-12-11 · Wingderm Electro Optics
Reason: All model WLA-01 systems sold to US customers are found to have labeling non-compliances - Non-ablative Fractional Laser Systems, Model: WFB-01
FDA Device · Class II · 2024-12-11 · Wingderm Electro Optics
Reason: Model WFB-01 sold to US customers before Aug 23, 2022 has been found to have a software bug (6 units). All WFB-01 models sold to US customers found to have labeling non-compliances (22 units)