FDAAugust 22, 2024device
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.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
kinova
Recall history
No related federal recalls on record for this brand yet.
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