FDA Device recall Z-2129-2014
Darby Dental Supply Compolite Bond SE Self-Etch/Light-Curing
- FDA Device
- Class II
- terminated
- Published 2014-08-06
On 2014-08-06 the FDA classified a Class II recall of Darby Dental Supply Compolite Bond SE Self-Etch/Light-Curing by Novocol, citing septodont is recalling Self-Etch bond because the material was incorrectly packaged.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2129-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-16 |
| Published | 2014-08-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Novocol |
| Distribution | NY, PA, VA |
Product
Darby Dental Supply Compolite Bond SE Self-Etch/Light-Curing. This product is used to adhere restorative material to the tooth during restorations. Package contains 100 0.125 mL unit dose tips, 100 applicator brushes, and a product insert.
Reason
Septodont is recalling Self-Etch bond because the material was incorrectly packaged.
Identifiers
| code_info | Product Order Number 950-9119; Lot Number C4211-3; UPC Code *950-9119*; Expiration Date September 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-2129-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.