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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Home Healthcare

Kinova Inc: Jaco Assistive Robot Arms Recalled for Potential Fire Hazard

Agency Publication Date: October 11, 2024
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Summary

Kinova Inc is recalling approximately 949 KINOVA Jaco assistive robot arms because of a potential installation issue that can lead to a fire. These devices, which are designed to replace upper limb functions for individuals, may pose a risk if the arm becomes damaged and comes into contact with a wheelchair that has electrical leakage. This recall affects models PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, and KR MJ2 0001, which were distributed worldwide including several U.S. states.

Risk

A fire can occur if a damaged Jaco robotic arm interacts with a wheelchair exhibiting electrical leakage. This combination of hardware damage and electrical failure could lead to overheating or sparking, potentially causing serious burns or property damage.

What You Should Do

  1. Identify if your device is affected by checking the model number on your Jaco robotic arm. Affected models include: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, and KR MJ2 0001.
  2. Check the robot arm for any visible signs of damage, such as cracks, exposed wiring, or loose parts.
  3. Contact your healthcare provider or equipment specialist to ensure your wheelchair is not exhibiting any electrical leakage issues that could interact with the device.
  4. Contact Kinova Inc directly at their headquarters at 355 Peel St Suite 301, Montreal, Canada, or reach out to your local authorized distributor for further instructions and to schedule an inspection of the installation.
  5. Discuss with your healthcare provider if you should continue using the device while waiting for a safety inspection.
  6. For additional questions or to report a safety concern, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action

Professional inspection and guidance

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund.

Affected Products

Product: KINOVA Jaco assistive robot
Model / REF:
PJ 0000 0001
PJ 0000 0012
PJ 0090 0001
PJ 0090 0006
KR MJ2 0001
Lot Numbers:
All lot numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95065
Status: Active
Manufacturer: Kinova Inc
Sold By: Authorized medical device distributors
Manufactured In: Canada
Units Affected: 949 units
Distributed To: California, Missouri, North Carolina, Ohio

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.