FDA Device recall Z-0376-2014
ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations
- FDA Device
- Class II
- terminated
- Published 2013-11-27
On 2013-11-27 the FDA classified a Class II recall of ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations by Ivoclar Vivadent, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0376-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-23 |
| Published | 2013-11-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ivoclar Vivadent |
| Distribution | AZ, CA, IA, IL, IN, LA, NJ, NY, OR, PA, SC, TX, WA, WI |
Product
ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations
Reason
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.
Identifiers
| code_info | Product Code 630378AN; Lot Number: R59595; Expiration date of 3 January 2015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0376-2014%22
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