Device recall
Z-0199-2016: Robotic hand accessory to InMotion Arm, rehabilitation robot.
FDA device recall · Class II · Interactive Motion Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0199-2016 |
|---|---|
| Recall event | 72326 |
| Product | Robotic hand accessory to InMotion Arm, rehabilitation robot. |
| Product code | IKK |
| Recalling firm | Interactive Motion Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 13, 2017 |
| FEI number | 3002758968 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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