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

Recall Z-0376-2014 — ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations

U.S. FDA — Device Enforcement · United States · 2013-09-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0376-2014
Date of alert
2013-09-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ivoclar Vivadent, Inc.
Product category
device
Product type
Devices
Reported risk: Ivoclar Vivadent, Inc. is recalling a lot of ExciTE F DSC Dental Adhesive found to produce a blue green discoloration when used in combination with cements.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.