NVM5 1025906Recalls & reported problems
Nuvasive, Inc. · NVM5 Dual Needle Electrode, 2 Pack · 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 00887517075338), received between May 21, 2021 and May 21, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
1 other recall cover devices cleared under the same FDA submission (K143641); they may or may not involve this specific model.
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
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
ON (B)(6) 2021 A PATIENT UNDERWENT A SPINAL PROCEDURE UTILIZING NEURO MONITORING WHERE NEEDLES WERE PLACED FOR STIMULATION. THE CASE WAS COMPLETED WITH NO ISSUE BUT UPON REMOVAL OF THE NEEDLES ONE WAS OBSERVED TO BE MISSING. THE MISSING NEEDLE WAS LOCATED IN THE PATIENT VIA X-RAY BUT THE SURGEON DECIDED LEAVE THE DEVICE AS IS IN-SITU. THE PATIENT WAS INFORMED POST-OP OF THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11866466 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K143641. One submission often covers many models, so check the product and lot details in each record.
- Z-2684-2020 · Jun 10, 2020 · TerminatedNuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal s
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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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