Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1076-2013 — 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.

U.S. FDA — Device Enforcement · United States · 2013-02-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1076-2013
Date of alert
2013-02-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical
Product category
device
Product type
Devices
Reported risk: Kerr Corporation is initiating this recall because raw material used to produce the Maxcem Elite is causing the material to prematurely polymerize in the syringe. The product could be difficult to extrude or demonstrate a shorter work-time as the material may prematurely set prior to placing restorations on the tooth or core build-up. As a result, the restoration may not be seated properly.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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