Device recall
Z-0233-2009: PREMISE, PART NO. 32654, 10 PACK UNIDOSE PREMISE A4, dental composite
FDA device recall · Class II · Kerr Corp
Key facts
| Recall number (Z-number) | Z-0233-2009 |
|---|---|
| Recall event | 49506 |
| Product | PREMISE, PART NO. 32654, 10 PACK UNIDOSE PREMISE A4, dental composite |
| Product code | EBF |
| Recalling firm | Kerr Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2012 |
| 510(k) numbers | K060472 |
| FEI number | 2024312 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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