Device recall
Z-0859-2012: Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro Whitening…
FDA device recall · Class II · Church & Dwight Inc
Key facts
| Recall number (Z-number) | Z-0859-2012 |
|---|---|
| Recall event | 60853 |
| Product | Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro Whitening Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal. |
| Product code | JEQ |
| Recalling firm | Church & Dwight Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2015 |
| FEI number | 2280705 |
At a glance
- None 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