Reported Oct 23, 2024 · Ongoing

KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco…

Kinova Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Kinova Inc · 355 Peel St Suite 301 · Montreal · N/A

Is this the product you have?

  • KINOVA Jaco assistive robot
  • Model NumbersPJ 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
Lot codes and dates
  • Model Numbers
    • PJ 0000 0001
    • PJ 0000 0012
    • PJ 0090 0001
    • PJ 0090 0006
    • KR MJ2 0001. All lot numbers
Amount recalled
949 units

Where it was sold

Why it was recalled

Stop using this product now

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.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.