--- title: "WINGDERM ELECTRO-OPTICS LTD. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search WINGDERM ELECTRO-OPTICS LTD. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/wingderm-electro-optics-ltd/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # WINGDERM ELECTRO-OPTICS LTD. recall records **2** reported ongoing 2 records in this archive. Latest source date Aug 23, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. 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/). ## Records and reported status Aug 23, 2024 FDA device enforcement ### [Non-ablative Fractional Laser Systems, Model: WFB-01](https://isitonrecall.com/recall/fda-device-z-0555-2025-non-ablative-fractional-laser-systems-model-wfb-01/) 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) Class II Reported ongoing Distribution: Worldwide Distribution [Official source for Non-ablative Fractional Laser Systems, Model: WFB-01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0555-2025%22) Aug 23, 2024 FDA device enforcement ### [Diode Laser Hair Removal model: WLA-01](https://isitonrecall.com/recall/fda-device-z-0556-2025-diode-laser-hair-removal-model-wla-01/) All model WLA-01 systems sold to US customers are found to have labeling non-compliances Class II Reported ongoing Distribution: Worldwide Distribution [Official source for Diode Laser Hair Removal model: WLA-01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0556-2025%22) ## Reasons in these listed records - 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) - All model WLA-01 systems sold to US customers are found to have labeling non-compliances These examples come from this result page and are not a ranking of every recall reason. ## Checking WINGDERM ELECTRO-OPTICS LTD. ### Is there a recall on wingderm electro-optics ltd. right now? This archive contains 2 records, including 2 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search WINGDERM ELECTRO-OPTICS LTD.](https://isitonrecall.com/check/?q=WINGDERM%20ELECTRO-OPTICS%20LTD.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)