Recall
Robotic hand accessory to InMotion Arm, rehabilitation robot.
Interactive Motion Technologies, Inc. · 5 May 2012
- Status
- Recall terminated
- Why, in the FDA's words
- “Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.”
- Recall began
- 5 May 2012
- Company
- Interactive Motion Technologies, Inc.
- Device type
- Product code (IKK)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.