NVM5 NVM5MULTIEVALRecalls & reported problems
Nuvasive, Inc. · NVM5 Eval EMG_MEP_SSEP Bendini & NMOR · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517973405), received between Aug 25, 2025 and Aug 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Communication or Transmission Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Communication or Transmission Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 25, 2025Communication or Transmission Problem; Adverse Event Without Identified Device or Use Problem; Communication or Transmission Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT HAD BURNS POST SURGERY USING NVM5 ELECTRODES.
Patient problems: Burn(s)
MAUDE report 22882788 ↗
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- SENTIO 286202108Medos International Sàrl · Neurosurgical nerve locator2 reports
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- Boston Endo Surgical Technologies LLC PK1015Lacey Manufacturing Company, LLC · Neurosurgical Nerve Locator1 report
- ALARA Neuro Access Needle Kit AAN-09-2NSSurgentec, LLC · Neurosurgical Nerve Locator1 report
- BMAN Solid Diamond Needle SR07-1100Surgentec, LLC · Neurosurgical Nerve Locator1 report
- NVM5 2023000Nuvasive, Inc. · Neurosurgical nerve locator1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.