Klowen Braces recalls KL Owen Custom Orthodontic Solution model CIAS-800033 due to potential incorrect bracket placement. Affected units include specific lot numbers and UDI/DI codes.
A product error defect may cause incorrect bracket placement.
Klowen Braces is recalling their KL Owen Custom Orthodontic Solution model CIAS-800033 because a manufacturing error might cause incorrect bracket placement. This could lead to improper tooth alignment or discomfort for users.
A manufacturing error in the product can cause brackets to be placed incorrectly on teeth. This might result in improper tooth alignment or discomfort during treatment.
Orthodontic patients who own the KL Owen Custom Orthodontic Solution model CIAS-800033 with the listed lot numbers or UDI/DI codes are affected. Patients using the product for dental treatment are most at risk.
Check for the model number CIAS-800033 on the product. Look for the specific lot numbers: 1779407586392-0, 1779138889952-0, or 1778173992342-0. The UDI/DI code 10850061082029 is also associated with this recall.
Verify the model number CIAS-800033 and lot numbers listed in the recall notice.
The recalled model is KL Owen Custom Orthodontic Solution with catalog number CIAS-800033.
The affected lot numbers are 1779407586392-0, 1779138889952-0, and 1778173992342-0.
The recall notice does not specify a remedy, so no action is required beyond checking if the product is affected.
We’ve drafted a message you can send Klowen Braces to request your refund or repair — edit it as you like.
Subject: Recall Z-2699-2026 — Klowen Braces Klowen Braces Hello, I own a Klowen Braces that is covered by recall Z-2699-2026 from Klowen Braces. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.