FDA
Food and Drug Administration · Recall Z-2699-2026 · Jun 8, 2026KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
Klowen Braces
The hazard
A product error defect may cause incorrect bracket placement. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI/DI 10850061082029Model Lot Numbers: 1779407586392-0Model 1779138889952-0Model 1778173992342-0UPC 10850061082029UPC 1779407586392UPC 1779138889952UPC 1778173992342Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.