Device recall
Z-1115-2012: Brand Name: Fusio Liquid Dentin, part number N21SB, N21SC. Product Usage: The…
FDA device recall · Class II · Kerr Corporation
Key facts
| Recall number (Z-number) | Z-1115-2012 |
|---|---|
| Recall event | 61239 |
| Product | Brand Name: Fusio Liquid Dentin, part number N21SB, N21SC. Product Usage: The intended use of this device is as a self-etch, self-adhesive flowable resin composite indicated for light-cured dental restorations. Applications include self-etch base liner, restorations of carious lesions, Class I, III… |
| Product code | EBF |
| Recalling firm | Kerr Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 28, 2012 |
| 510(k) numbers | K072545 |
| FEI number | 2024312 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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