Integra LifeSciences Corp. (NeuroSciences) has recalled 1,198 units of the TruDi Navigation System - Multi Instrument Adapter. When used with a Patient Tracker, certain versions of this adapter may fail to provide accurate visual verification of a device's location within a patient's body during surgery. Healthcare providers should verify their equipment and contact the manufacturer to ensure the system meets accuracy specifications.
The navigation system may provide inaccurate visual data regarding where a medical device is located inside a patient's anatomy. This inaccuracy could lead to instruments being placed incorrectly during sensitive surgical procedures, potentially resulting in patient harm.
Manufacturer correction or return
Recall #: Z-0420-2026. Affected when used together with the Patient Tracker.
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 · Raw API Response
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