Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001 Recalled by Kinova Inc Due to Potential installation issue that could result in a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Kinova Inc directly.
Affected Products
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.
Quantity: 949 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Kinova Inc
Kinova Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report