Brand

Kerr/pentron, Dba Kerr Corporation And Pentron Clinical Recalls

4 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Kerr/pentron, Dba Kerr Corporation And Pentron Clinical.

4Total Recalls
0Critical
73,031Units Affected
Feb 25, 2020Most Recent
All Recalls

Every Kerr/pentron, Dba Kerr Corporation And Pentron Clinical Recall

Sorted by most recent. Click any recall for full details.

4 recalls
High RiskFDA
Kerr/pentron, Dba Kerr Corporation And Pentron Clinical
Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The intended use of th...
Medical Implants·111 affected·Feb 25, 2020
High RiskFDA
Kerr/pentron, Dba Kerr Corporation And Pentron Clinical
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Medical Devices·31,904 affected·Jul 13, 2018
High RiskFDA
Kerr/pentron, Dba Kerr Corporation And Pentron Clinical
NX3 Try-In Gel. The product is used as a tooth shade resin material.
Medical Devices·197 affected·Sep 13, 2013
High RiskFDA
Kerr/pentron, Dba Kerr Corporation And Pentron Clinical
Kerr Maxcem Elite, self-etch/self-adhesive resin cement; Intro Kit Part No. 34417; DMC 0446 Rev 0. Used for cementation of all indirec...
Medical Devices·40,819 affected·Feb 22, 2013