Kinova Inc

1 FDA enforcement actions

1 Total Recalls

1 Class I

0 Class II

0 Class III

Firm Details

Product Types: device
States: N/A

All Recalls

Class I: Dangerous 08/22/2024 device

Potential installation issue that could result in a fire hazard in the event of an interaction between a damaged Jaco arm and a wheelchair exhibiting electrical leakage.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.