Drug recall
Robotic hand accessory to InMotion Arm, rehabilitation robot.
FDA recall event 72326 · Class II · Interactive Motion Technologies, Inc.
Key facts
| Event ID | 72326 |
|---|---|
| Recall numbers | Z-0199-2016 |
| Recalling firm | Interactive Motion Technologies, Inc. |
| Product type | Devices |
| Products | Robotic hand accessory to InMotion Arm, rehabilitation robot. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard. |
| Initiation date | May 5, 2012 |
| Report date | Nov 11, 2015 |
| Termination date | Jul 13, 2017 |
| City | Watertown |
| State | MA |
| Country | United States |
| FEI number | 3002758968 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: