Robotic hand accessory to InMotion Arm — Class II medical device recall Z-0199-2016
Terminated recall by Interactive Motion Technologies, Inc., reported 2015-11-11, distributed in TN, TX. Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a
| Recall number | Z-0199-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Interactive Motion Technologies, Inc., Watertown, MA, United States |
| Recall initiated | 2012-05-05 |
| Classified | 2015-11-02 |
| Reported by FDA | 2015-11-11 |
| Terminated | 2017-07-13 |
| Distributed | TN, TX |
| Countries outside the US | AT, BR, CN, HK, KR |
| Quantity | 8 |
| Serial numbers | H006, H007, H019, H020, H021, H022, H023, H024 |
Product
Robotic hand accessory to InMotion Arm, rehabilitation robot.
Reason for recall
Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0199-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.