Recall Z-0199-2016— Interactive Motion Technologies, Inc.
Class II · Terminated
Class II FDA medical device recall by Interactive Motion Technologies, Inc., initiated 2012-05-05, terminated 2017-07-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Robotic hand accessory to InMotion Arm, rehabilitation robot.. Reason: Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard..
- Recalling firm
- Interactive Motion Technologies, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-05-05
- Terminated
- 2017-07-13
- Firm location
- Watertown, MA, United States
Product description
Robotic hand accessory to InMotion Arm, rehabilitation robot.
Reason for recall
Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.
Data sourced from openFDA. This site is unofficial and independent of the FDA.