Device brand name · Stimulator nerve
Nim Emg - Endotracheal Tube - Nim Flex: medical device reports filed with FDA
170 reports name it, 2015–2026. Manufacturer given most often on reports: Medtronic Xomed. Product code ETN.
- 170
- device reports naming the brand
- 0% of all MAUDE reports · about 15 a year
- 39
- reports, 12 months to August 2026
- 38 in the 12 months before
- 77.1%
- classified as malfunction
- 83.4% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
170 medical device reports received by FDA name the brand "Nim Emg - Endotracheal Tube - Nim Flex" (stimulator nerve); the manufacturer given most often on reports is Medtronic Xomed; received from February 2015 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
39 reports arrived in the 12 months to August 2026, close to the 38 of the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (77.1%) and injury (22.9%); across all stimulator, nerve reports (product code ETN) death is recorded in 0.2% and malfunction in 83.4%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are incorrect, inadequate or imprecise result or readings (31.8%), circuit failure (11.8%) and unintended deflation (11.8%). The patient problems coded most often are unintended extubation, extubate and airway obstruction. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 5,123 reports carrying product code ETN. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Incorrect, inadequate or imprecise result or readings | 54 | 31.8% | 26.8% |
| Circuit failure | 20 | 11.8% | 0.8% |
| Unintended deflation | 20 | 11.8% | 8.8% |
| Partial blockage | 8 | 4.7% | 0.6% |
| Breakthe device broke | 6 | 3.5% | 2.9% |
| Obstruction of flow | 6 | 3.5% | 2.5% |
| Device sensing problem | 5 | 2.9% | 3.8% |
| Occlusion within devicethe device blocked | 5 | 2.9% | 0.4% |
| Deflation problem | 3 | 1.8% | 0.2% |
| Detachment of device or device componentpart of the device came off | 3 | 1.8% | 0.2% |
| Device operates differently than expectedthe device behaved unexpectedly | 3 | 1.8% | 8.3% |
| Difficult to insertthe device was hard to insert | 3 | 1.8% | 0.3% |
| False negative result | 3 | 1.8% | 7% |
| Fitting problem | 3 | 1.8% | 0.1% |
| Inappropriate audible prompt/feedback | 3 | 1.8% | 5.2% |
| Leak/splashthe device leaked | 3 | 1.8% | 2.4% |
| Material puncture/hole | 3 | 1.8% | 1.2% |
| Material protrusion/extrusion | 2 | 1.2% | 0.5% |
| No device output | 2 | 1.2% | 0.2% |
| No display/image | 2 | 1.2% | 0.2% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Unintended extubation | 29 | 17.1% |
| Extubate | 17 | 10% |
| Airway obstruction | 5 | 2.9% |
| Low oxygen saturation | 3 | 1.8% |
| Occlusion | 3 | 1.8% |
| Paralysis | 3 | 1.8% |
| Respiratory distressdifficulty breathing | 3 | 1.8% |
| Wheezingwheezing | 2 | 1.2% |
| Apnea | 1 | 0.6% |
| Bronchospasmtightening of the airways | 1 | 0.6% |
| Burn(s)a burn | 1 | 0.6% |
| Dyspneashortness of breath | 1 | 0.6% |
| Hemoptysis | 1 | 0.6% |
| Hypoventilation | 1 | 0.6% |
| Low blood pressure/ hypotension | 1 | 0.6% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Nim Emg - Endotracheal Tube - Nim Flex | Product code ETN | All MAUDE reports |
|---|---|---|---|
| Reports | 170 | 5,123 | 26,136,888 |
| Share of that pool | — | 3.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 2 | 9 |
| Classified as injury | 22.9% | 15.8% | 36.2% |
| Classified as malfunction | 77.1% | 83.4% | 62.3% |
| Filed by the manufacturer | 100% | 96.6% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code ETN
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Nim Emg - Endotracheal Tube - Trivantage | 976 | 224 | 0.1% |
| Nim Emg - Endotracheal Tube | 540 | 1 | 0.6% |
| Nim 3 0 Mainframe International | 560 | 69 | 0% |
| Nim 3 0 Interface | 472 | 48 | 0% |
| Nim 3 0 Mainframe | 407 | 39 | 0% |
| Nim Probe | 369 | 78 | 0% |
| Nim-Neuro 3 0 Mainframe | 212 | 38 | 0% |
| Nim Vital Patient Interface 4 Channel | 209 | 123 | 0% |
| Patient Interface Nim4cpb1 Nim 4 0 | 298 | 122 | 0% |
| Nim 4 0 Console | 1,438 | 528 | 0% |
| Medtronic | 2,953 | 17 | 4.4% |
| Nuvasive Reline System | 468 | 8 | 1.5% |
| Viking | 181 | 1 | 5% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Nim Emg - Endotracheal Tube - Nim Flex reports
How many FDA reports name Nim Emg - Endotracheal Tube - Nim Flex?
170 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 39 in the latest 12 months.
What kinds of events are reported?
malfunction (77.1%) and injury (22.9%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
incorrect, inadequate or imprecise result or readings (31.8%), circuit failure (11.8%), unintended deflation (11.8%), partial blockage (4.7%) and break (3.5%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Nim Emg - Endotracheal Tube - Nim Flex was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.