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NA 2010770Recalls & reported problems

Nuvasive, Inc. · EMG ET Tube, 7mm ID Long Electrode · 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 00887517055637), received between Nov 18, 2019 and Nov 18, 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Deflation Problem1

Patient problems

  • No Code Available1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 18, 2019Deflation Problem; Deflation Problem

    SUPPLEMENTAL REPORT, UPDATED DATA IN FIELDS.

    Patient problems: No Code Available; No Consequences Or Impact To Patient

    MAUDE report 9339128 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.