Devices › Stimulator, hypoglossal nerve, implanted, apnea
Device brand name · Inspire v ipg model 3150
Inspire V IPG Model 3150: medical device reports filed with FDA
166 reports name it, 2025–2026. Manufacturer given most often on reports: Inspire Medical Systems. Product code MNQ.
- 166
- device reports naming the brand
- 0% of all MAUDE reports · about 166 a year
- 163
- reports, 12 months to August 2026
- 3 in the 12 months before
- 0%
- classified as malfunction
- 4.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 166 reports that name the brand "Inspire V IPG Model 3150" (inspire v ipg model 3150), received between July 2025 and August 2026; the manufacturer given most often on reports is Inspire Medical Systems. Spellings of one product vary from report to report.
163 reports arrived in the 12 months to August 2026, up 5333% from 3 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 injury (100%); across all stimulator, hypoglossal nerve, implanted, apnea reports (product code MNQ) death is recorded in 0.1% and malfunction in 4.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are migration (17.5%), migration or expulsion of device (2.4%) and expulsion (1.8%). The patient problems coded most often are wound dehiscence, inflammation and hematoma. 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.
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 3,571 reports carrying product code MNQ. 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 |
|---|---|---|---|
| Migrationthe device moved from where it was placed | 29 | 17.5% | 6% |
| Migration or expulsion of device | 4 | 2.4% | 4.6% |
| Expulsion | 3 | 1.8% | 1.4% |
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 |
|---|---|---|
| Wound dehiscencea wound reopened | 28 | 16.9% |
| Inflammationinflammation | 27 | 16.3% |
| Hematomaa collection of blood under the skin or in tissue | 26 | 15.7% |
| Medical device site infectioninfection at the device site | 24 | 14.5% |
| Painpain, site not specified | 23 | 13.9% |
| Purulent discharge | 18 | 10.8% |
| Fluid discharge | 16 | 9.6% |
| Swelling/ edema | 14 | 8.4% |
| Implant pain | 13 | 7.8% |
| Seromaa collection of fluid under the skin | 8 | 4.8% |
| Twiddlers syndrome | 4 | 2.4% |
| Erosion | 3 | 1.8% |
| Pocket erosion | 3 | 1.8% |
| Rashskin rash | 3 | 1.8% |
| Abscessa collection of pus | 2 | 1.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Inspire V IPG Model 3150 | Product code MNQ | All MAUDE reports |
|---|---|---|---|
| Reports | 166 | 3,571 | 26,136,888 |
| Share of that pool | — | 4.6% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 100% | 95.3% | 36.2% |
| Classified as malfunction | 0% | 4.5% | 62.3% |
| Filed by the manufacturer | 100% | 95% | 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 MNQ
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Inspire Model 3028 IPG | 1,437 | 298 | 0.3% |
| Inspire Model 4063 Stimulation Lead | 1,313 | 426 | 0% |
| Inspire Model 4340 Respiratory Sensing Lead | 272 | 36 | 0% |
| Dexcom G7 | 1,394 | 583 | 0.1% |
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 Inspire V IPG Model 3150 reports
How many FDA reports name Inspire V IPG Model 3150?
166 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 163 in the latest 12 months.
What kinds of events are reported?
injury (100%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
migration (17.5%), migration or expulsion of device (2.4%) and expulsion (1.8%). 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 Inspire V IPG Model 3150 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.