Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module kit intended for intraoperative...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact NuVasive Inc directly.
Affected Products
Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.
Quantity: 23
Why Was This Recalled?
The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the correct part number 1747065, NVM5 Harness, Gen 3.5 EM. This issue can result in delay in therapy or lack of EMG neuromonitoring during surgery if the surgeon elects to proceed without the NVM5.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About NuVasive Inc
NuVasive Inc has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report