CLASS II Device recall · Reported 11 Nov 2015 · FDA Enforcement Report

Robotic hand accessory to InMotion Arm, rehabilitation robot recalled

Interactive Motion Technologies is recalling Robotic hand accessory to InMotion Arm, rehabilitation robot, distributed in Tennessee, Texas. The recall was initiated on 5 May 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSerial 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)
Quantity recalled8

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-0199-2016
FDA event ID
72326
Recalling firm
Interactive Motion Technologies, Watertown, MA
Classification
Class II
Status
Terminated
Recall initiated
5 May 2012
FDA classified
2 Nov 2015
Reported
11 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

5 May 2012Recall initiated by company
2 Nov 2015Classified by FDA+1276 days
11 Nov 2015Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.

Product as listed by the FDA

Robotic hand accessory to InMotion Arm, rehabilitation robot.

Where it was 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.

TennesseeTexas

Questions about this recall

Is Robotic hand accessory to InMotion Arm, rehabilitation robot recalled?

Yes. Interactive Motion Technologies recalled Robotic hand accessory to InMotion Arm, rehabilitation robot on 5 May 2012. The recall is Class II and its status is Terminated. Recall number Z-0199-2016.

Why was it recalled?

Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.

Which lots are affected?

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)

Where was it sold?

Worldwide Distribution - US Distribution to the states of : Texas and Tennessee., and to the countries of : China, Brazil, Hong Kong, Austria and South Korea.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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