Device recall
Z-0766-2013: P10 Tobii battery box (product number 510410) Product Usage - Battery pack for…
FDA device recall · Class II · Tobii Assistive Technology, Inc.
Key facts
| Recall number (Z-number) | Z-0766-2013 |
|---|---|
| Recall event | 64099 |
| Product | P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device. MyTobii P10 is a portable eye-controlled communication device featuring the Tobii Eye Control system. |
| Product code | ILQ |
| Recalling firm | Tobii Assistive Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 2016 |
| FEI number | 3007873415 |
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