Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical Due to An issue within production process used to package...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical directly.
Affected Products
Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The intended use of this device is to be used for the cementation of indirect restorations including veneers, inlays, onlays, bridges, posts, and the cementation of crown restorations to implant abutments.
Quantity: 111 kits
Why Was This Recalled?
An issue within production process used to package trial kits let to the inclusion of the incorrect bonding agent for the kit. Use of the incorrect bonding agent may lead to increased risk of bond failures.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report