Z-2699-2026 Class II Ongoing
FDA device recall Z-2699-2026 was initiated by Klowen Braces on June 8, 2026 and is designated Class II. Reason for recall: A product error defect may cause incorrect bracket placement. The recall status is ongoing. Affected quantity: 3 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 15, 2026
- Initiation Date
- June 8, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3 units
Product Description
KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
Reason for Recall
A product error defect may cause incorrect bracket placement.
Distribution Pattern
US Nationwide distribution in the states of OH, TX, SC VA.
Code Information
UDI/DI 10850061082029, Lot Numbers: 1779407586392-0, 1779138889952-0, 1778173992342-0