Recall Z-2699-2026— Klowen Braces
Class II · Ongoing
Class II FDA medical device recall by Klowen Braces, initiated 2026-06-08. Product: KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,. Reason: A product error defect may cause incorrect bracket placement..
- Recalling firm
- Klowen Braces
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-06-08
- Firm location
- Richardson, TX, United States
Product description
KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
Reason for recall
A product error defect may cause incorrect bracket placement.
Data sourced from openFDA. This site is unofficial and independent of the FDA.