NA 2010380Recalls & reported problems
Nuvasive, Inc. · NV ET Tube, 8mm EMG ID · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00887517161390), received between Mar 2, 2019 and Mar 2, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Deflation 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Deflation Problem1
Patient problems
- Extubate1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 2, 2019Deflation Problem; Deflation Problem
ON (B)(6) 2019 PATIENT UNDERWENT A TOTAL THYROIDECTOMY PROCEDURE IN WHICH A NUVASIVE NV ET TUBE WAS UTILIZED. IT WAS REPORTED THAT THE ET TUBE'S CUFF WAS NOT HOLDING PRESSURE DURING PROCEDURE. THE ET TUBE WAS REPLACED AND THE ISSUE WAS RESOLVED. NO PATIENT INJURY REPORTED.
Patient problems: Extubate
MAUDE report 8384785 ↗
Other Neurosurgical nerve locator devices
- Arcus 16122-02-SAlphatec Spine, Inc. · Neurosurgical nerve locator4 reports
- Arcus 16122-01-SAlphatec Spine, Inc. · Neurosurgical nerve locator4 reports
- SENTIO 286202400Medos International Sàrl · Neurosurgical nerve locator2 reports
- SENTIO 286202108Medos International Sàrl · Neurosurgical nerve locator2 reports
- NVM5 NVM5MULTIEVALNuvasive, Inc. · Neurosurgical nerve locator1 report
- ALARA Neuro Access Needle Kit AAN-09-2NSSurgentec, LLC · Neurosurgical Nerve Locator1 report
- Neurosign V4 Intraoperative Nerve Monitor 4230-00The Magstim Company Limited · Neurosurgical Nerve Locator1 report
- SentioMMG 2006Innovative Surgical Solutions LLC · Neurosurgical Nerve Locator1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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