Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical: Medical Device Recalls in 2013

According to to data from the FDA, there were 2 medical device recalls made by Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical in 2013. See the details of the recalls below.

You can see similar recalls for other firms.

• Kerr Maxcem Elite, self-etch/self-adhesive resin cement; Intro Kit Part No. 34417; DMC 0446 Rev 0. Used for cementation of all indirect restorations.
• NX3 Try-In Gel. The product is used as a tooth shade resin material.