Interactive Motion Technologies, Inc. recalls Robotic hand accessory to InMotion Arm, rehabilitation robot.
- Recall date
- May 5, 2012
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0199-2016
- FDA classification
- Class II
- Brand / firm
- Interactive Motion Technologies, Inc.
- Sold / distributed
- Worldwide Distribution - US Distribution to the states of : Texas and Tennessee., and to the countries of : China, Brazil, Hong Kong, Austria and South Korea.
Why it was recalled
Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Robotic hand accessory to InMotion Arm, rehabilitation robot.
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