FDA Class II · Medical device · July 15, 2026
KL Owen Custom Orthodontic Solution recall — Klowen Braces
A product error defect may cause incorrect bracket placement.
Official ID Z-2699-2026 · Official record ↗
Recall found. Klowen Braces is named in FDA Class II recall Z-2699-2026 covering KL Owen Custom Orthodontic Solution. Hazard: A product error defect may cause incorrect bracket placement. Identifying details: UDI/DI 10850061082029, Lot Numbers: 1779407586392-0, 1779138889952-0, 1778173992342-0. Status: Ongoing.
A product error defect may cause incorrect bracket placement.
Official ID Z-2699-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.