Device recall
Z-0074-2010: Kerr TempBond Clear, Part # 33351, 1717 West Collins Avenue, Orange, CA 92867…
FDA device recall · Class III · Kerr Corp
Key facts
| Recall number (Z-number) | Z-0074-2010 |
|---|---|
| Recall event | 53296 |
| Product | Kerr TempBond Clear, Part # 33351, 1717 West Collins Avenue, Orange, CA 92867. Intended for use in a dual-cured, temporary resin-based cement designed to be used in conjunction with temporary restoration such as crowns, bridges, inlays and onlays. |
| Product code | EMA |
| Recalling firm | Kerr Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 12, 2011 |
| 510(k) numbers | K982590 |
| 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