Intuitive Surgical, Inc. is recalling 1,167,860 reusable surgical instruments with jaws used with robotic surgical systems. The recall was initiated because the grip cables used to operate the instrument jaws can fray or break during use. This affects various 8mm surgical tools, including scissors, forceps, needle drivers, and retractors. While no specific patient injuries were reported in this announcement, the manufacturer is taking action due to an increased rate of complaints regarding these broken cables.
If a grip cable frays or breaks during surgery, the instrument may fail to function correctly or small metal fragments could potentially shed into the patient. This defect could lead to surgical delays while the tool is replaced or increase the risk of procedural complications.
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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.
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.