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[Recalled] Robotic hand accessory to InMotion Arm, rehabilitation robot. — Unsupervised patient could potentially mis-use the device and remove or rotate… | FDA 2012-05-05

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductRobotic hand accessory to InMotion Arm, rehabilitation robot.
Brand / manufacturerInteractive Motion Technologies, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0199-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date05 May 2012

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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