Nim Vital Patient Interface 4 Channel: medical device reports filed with FDA

209 reports name it, 2024–2026. Manufacturer given most often on reports: Medtronic Xomed. Product code GWF.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "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."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

209
device reports naming the brand: 0% of all MAUDE reports · about 84 a year; 123
reports, 12 months to August 2026: 60 in the 12 months before; 100%
classified as malfunction: 96.1% across the product code; 0%
classified as death, as reported: 0 reports · not verified by FDA

FDA's MAUDE database holds 209 reports that name the brand "Nim Vital Patient Interface 4 Channel" (stimulator electrical evoked response), received between January 2024 and August 2026; the manufacturer given most often on reports is Medtronic Xomed. Spellings of one product vary from report to report.

123 reports arrived in the 12 months to August 2026, up 105% from 60 in 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 (100%); across all stimulator, electrical, evoked response reports (product code GWF) death is recorded in 0% and malfunction in 96.1%. 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 (90.9%), inappropriate audible prompt/feedback (10.5%) and false negative result (3.3%). 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

Death0%0

Injury0%0

Malfunction100%209

Other0%0

Not given0%0

Who filed the report

Manufacturer report100%209

Voluntary report0%0

User facility report0%0

Distributor report0%0

Not given0%0

Grey bar: all 3,308 reports carrying product code GWF. 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	190	90.9%	49.5%
Inappropriate audible prompt/feedback	22	10.5%	9.1%
False negative result	7	3.3%	8.2%
Battery problema problem with the battery	4	1.9%	1.3%
Breakthe device broke	4	1.9%	1.6%
Failure to power up	4	1.9%	4.1%
Problem with software installation	4	1.9%	1.6%
Application program freezes or fails to launch	3	1.4%	1.9%
Connection problema connection problem	3	1.4%	2.4%
Electrical /electronic property probleman electrical or electronic problem	3	1.4%	1.2%
False positive result	3	1.4%	3.1%
Temperature problem	3	1.4%	0.3%
Computer software problema software problem	2	1%	3.4%
Incomplete or inadequate connection	2	1%	1.8%
Device misassembled during manufacturing /shipping	1	0.5%	0.4%
Loose or intermittent connection	1	0.5%	0.3%
Signal artifact/noise	1	0.5%	1.5%

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.

In context

Measure	Nim Vital Patient Interface 4 Channel	Product code GWF	All MAUDE reports
Reports	209	3,308	26,136,888
Share of that pool	—	6.3%	0%
Classified as death, per 1,000 reports	0	0	9
Classified as injury	0%	3.4%	36.2%
Classified as malfunction	100%	96.1%	62.3%
Filed by the manufacturer	100%	98.1%	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 GWF

Brand	Reports	Latest 12 months	Classified as death
Nim 4 0 Console	1,438	528	0%
Patient Interface Nim4cpb1 Nim 4 0	298	122	0%
Nim-Eclipse Controller	221	33	0%
Nim-Eclipse Preamplifier	153	35	0%
Nim 3 0 Interface	472	48	0%
Nim 3 0 Mainframe International	560	69	0%
Nim 3 0 Mainframe	407	39	0%
Nim-Neuro 3 0 Mainframe	212	38	0%
Bravo	11,648	568	0%

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 Vital Patient Interface 4 Channel reports

How many FDA reports name Nim Vital Patient Interface 4 Channel?

209 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 123 in the latest 12 months.

What kinds of events are reported?

malfunction (100%). "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 (90.9%), inappropriate audible prompt/feedback (10.5%), false negative result (3.3%), battery problem (1.9%) and break (1.9%). 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 Vital Patient Interface 4 Channel 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.