FDA Device recall Z-0199-2016
Robotic hand accessory to InMotion Arm, rehabilitation robot
- FDA Device
- Class II
- terminated
- Published 2015-11-11
On 2015-11-11 the FDA classified a Class II recall of Robotic hand accessory to InMotion Arm, rehabilitation robot by Interactive Motion Technologies, citing unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0199-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-05-05 |
| Published | 2015-11-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Interactive Motion Technologies |
| Distribution | TN, TX |
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.
Identifiers
| code_info | Serial Numbers: H006, H007, H019, H020, H021, H022, H023, H024. Note: serial numbers may be written with an additional leading 0 (e.g. H0024 instead of H024) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0199-2016%22
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