# FDA device recall: KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,

> recall · VERIFIED · 2026-06-08

Firm: Klowen Braces · Class II · A product error defect may cause incorrect bracket placement.

- Company: Klowen Braces
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.