Device recall
Z-0376-2014: ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive…
FDA device recall · Class II · Ivoclar Vivadent, Inc.
Key facts
| Recall number (Z-number) | Z-0376-2014 |
|---|---|
| Recall event | 66359 |
| Product | ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations |
| Product code | MZW |
| Recalling firm | Ivoclar Vivadent, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 27, 2016 |
| 510(k) numbers | K093744 |
| FEI number | 1316092 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database