{
  "meta": {
    "disclaimer": "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. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "209236",
      "product_res_number": "Z-0049-2025",
      "event_date_initiated": "2024-08-22",
      "event_date_posted": "2024-10-11",
      "recall_status": "Open, Classified",
      "res_event_number": "95065",
      "product_code": "IQZ",
      "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.",
      "code_info": "Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001.  All lot numbers.",
      "firm_fei_number": "3009538853",
      "recalling_firm": "Kinova Inc",
      "address_1": "355 Peel St Suite 301 355 Peel St",
      "address_2": "Suite 301",
      "city": "Montreal",
      "country": "Canada",
      "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.",
      "root_cause_description": "Device Design",
      "action": "On 07/22/2024, Kinova notified consignees via UGENT: MEDICAL DEVICE CORRECTION letter.  Consignees were instructed contact Kinova immediately for an assessment, ensure that if the wheelchair is in contact with a damaged part of the Jaco arm in any position at any time, to unplug the Jaco arm from the power source immediately and contact Kinova, and read the updated user guide on Kinova's website.  Consignees were also requested to complete and return the acknowledgement and response form.\n\nDistributors were instructed to communicate the recall to all Jaco users, confirm receipt and understanding of the recall communication, maintain a detailed list of users, provide the user's contact details to Kinova, and perform an assessment for each user that response to the notification.  Distributors were also instructed to complete and return the acknowledgement and response form.",
      "product_quantity": "949 units",
      "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.",
      "openfda": {
        "device_name": "Hand, External Limb Component, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.3420",
        "device_class": "1",
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