ExciTE F DSC Soft touch Single Dose — Class II medical device recall Z-0376-2014
Terminated recall by Ivoclar Vivadent, Inc., reported 2013-11-27, distributed in AZ, CA, IA, IL, IN, LA, NJ, NY…. Ivoclar Vivadent, Inc. is recalling a lot of ExciTE F DSC Dental Adhesive found to produce a blue green discol
| Recall number | Z-0376-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ivoclar Vivadent, Inc., Buffalo, NY, United States |
| Recall initiated | 2013-09-23 |
| Classified | 2013-11-21 |
| Reported by FDA | 2013-11-27 |
| Terminated | 2016-05-27 |
| Distributed | AZ, CA, IA, IL, IN, LA, NJ, NY, OR, PA, SC, TX, WA, WI |
| Lot numbers | R59595 |
| Expiration dates | 2015-01-03 |
Product
ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0376-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.