Device recall
Z-0688-06: Tooth bonding resin. Optibond Solo Plus Dual Cure Kit, Part Number 31736, Lot…
FDA device recall · Class II · Kerr Corp
Key facts
| Recall number (Z-number) | Z-0688-06 |
|---|---|
| Recall event | 34769 |
| Product | Tooth bonding resin. Optibond Solo Plus Dual Cure Kit, Part Number 31736, Lot Number 427793 |
| Product code | KLE |
| Recalling firm | Kerr Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2012 |
| 510(k) numbers | K991808 |
| 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