Recalled NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with specific software versions v1.0.0, v1.1.1, v1.3.2, v1.4.3 may show false negative responses. Consumers should check their product details.
Potential for false negative response on the NIM Vital Nerve Monitoring System
Medtronic Xomed is recalling all NIM Vital Nerve Monitoring systems with specific software versions (v1.0.0, v1.1.1, v1.3.2, v1.4.3) that could show false negative responses. This means the system might not detect nerve issues properly, which could lead to missed medical conditions.
The system may show false negative responses, meaning it could fail to detect nerve issues that are actually present. This could lead to missed medical conditions if the system doesn't alert properly.
Users of the NIM Vital Nerve Monitoring system with the specified software versions and product models are affected. Patients using this system for nerve monitoring are most at risk.
Check if your NIM Vital Nerve Monitoring system has software versions v1.0.0, v1.1.1, v1.3.2, or v1.4.3. Look for product models including NIM4CM01, NIM4CM01RF, NIM4CPB1, or NIM4CPB1RF.
Identify your NIM Vital Nerve Monitoring system's software version and model number to see if it matches the recalled versions.
Software versions v1.0.0, v1.1.1, v1.3.2, and v1.4.3 are affected.
Check your product's software version and model number. Affected models include NIM4CM01, NIM4CM01RF, NIM4CPB1, and NIM4CPB1RF with the specified software versions.
No action is needed if your system does not match the recalled software versions or models.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-2409-2024 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-2409-2024 from Medtronic Xomed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
