Device recall
Z-0590-05: The product is a battery operated toothbrush. Spinbrush Pro Whitening Medium…
FDA device recall · Class II · Proctor & Gamble Co
Key facts
| Recall number (Z-number) | Z-0590-05 |
|---|---|
| Recall event | 31259 |
| Product | The product is a battery operated toothbrush. Spinbrush Pro Whitening Medium battery operated toothbrushes UPC 76687800193. |
| Product code | JEQ |
| Recalling firm | Proctor & Gamble Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2006 |
| FEI number | 1216894 |
At a glance
- None 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