Kinova Inc: Device Recall
Recall #Z-0049-2025 · 08/22/2024
Class I: Dangerous
Recall Details
- Recall Number
- Z-0049-2025
- Classification
- Class I
- Product Type
- Device
- Recalling Firm
- Kinova Inc
- Status
- Ongoing
- Date Initiated
- 08/22/2024
- Location
- Montreal, Canada
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 949 units
Reason for Recall
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.
Product Description
KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body.
Distribution Pattern
Worldwide - US Nationwide distribution in the states of California, Missouri, North Carolina, Ohio and the countries of Australia, Canada, China, Czechia, France, Germany, Netherlands, Norway, Portugal, Switzerland, Great Britain, Northern Ireland.
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.