Devices › Aortic valve, prosthesis, percutaneously delivered
Device brand name · Aortic valve prosthesis percutaneously delivered
Navitor Vision: medical device reports filed with FDA
2,045 reports name it, 2023–2026. Manufacturer given most often on reports: Abbott Medical. Product code NPT.
- 2,045
- device reports naming the brand
- 0% of all MAUDE reports · about 793 a year
- 1,258
- reports, 12 months to August 2026
- 676 in the 12 months before
- 7.4%
- classified as malfunction
- 15.2% across the product code
- 6.4%
- classified as death, as reported
- 131 reports · not verified by FDA
FDA's MAUDE database holds 2,045 reports that name the brand "Navitor Vision" (aortic valve prosthesis percutaneously delivered), received between December 2023 and August 2026; the manufacturer given most often on reports is Abbott Medical. Spellings of one product vary from report to report.
1,258 reports arrived in the 12 months to August 2026, up 86% from 676 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 (86.2%), malfunction (7.4%) and death (6.4%); across all aortic valve, prosthesis, percutaneously delivered reports (product code NPT) death is recorded in 10.1% and malfunction in 15.2%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are perivalvular leak (16.2%), migration or expulsion of device (14.3%) and difficult to fold, unfold or collapse (12.4%). The patient problems coded most often are heart block, aortic valve insufficiency/ regurgitation and low blood pressure/ hypotension. 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 79,063 reports carrying product code NPT. 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 |
|---|---|---|---|
| Perivalvular leak | 332 | 16.2% | 13% |
| Migration or expulsion of device | 293 | 14.3% | 2.4% |
| Difficult to fold, unfold or collapse | 254 | 12.4% | 0.5% |
| Improper or incorrect procedure or method | 140 | 6.8% | 0.5% |
| Intravalvular regurgitation | 83 | 4.1% | 3% |
| Off-label use | 55 | 2.7% | 0.2% |
| Material deformation | 45 | 2.2% | 1.6% |
| Patient device interaction problem | 40 | 2% | 11.9% |
| Patient-device incompatibilitythe device did not suit the patient | 24 | 1.2% | 0.3% |
| Incomplete coaptation | 21 | 1% | 0.7% |
| Separation problem | 21 | 1% | 0.1% |
| Device stenosis | 10 | 0.5% | 2.9% |
| Malposition of device | 9 | 0.4% | 5% |
| Premature separation | 6 | 0.3% | 0% |
| Device damaged by another device | 5 | 0.2% | 0.1% |
| Device difficult to setup or prepare | 3 | 0.1% | 0.3% |
| Insufficient device problem information | 3 | 0.1% | 10.2% |
| Material split, cut or torn | 2 | 0.1% | 1.2% |
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 |
|---|---|---|
| Heart block | 1,008 | 49.3% |
| Aortic valve insufficiency/ regurgitation | 200 | 9.8% |
| Low blood pressure/ hypotension | 146 | 7.1% |
| Stroke/cva | 126 | 6.2% |
| Arrhythmia | 113 | 5.5% |
| Cardiac arrestthe heart stopped | 83 | 4.1% |
| Pericardial effusionfluid around the heart | 60 | 2.9% |
| Movement disorder | 56 | 2.7% |
| Atrial fibrillationan irregular heart rhythm | 53 | 2.6% |
| Bradycardiaslow heart rate | 49 | 2.4% |
| Heart failure/congestive heart failure | 49 | 2.4% |
| Dyspneashortness of breath | 39 | 1.9% |
| Cardiac tamponade | 34 | 1.7% |
| Thrombosis/thrombus | 34 | 1.7% |
| Vascular dissection | 34 | 1.7% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Navitor Vision | Product code NPT | All MAUDE reports |
|---|---|---|---|
| Reports | 2,045 | 79,063 | 26,136,888 |
| Share of that pool | — | 2.6% | 0% |
| Classified as death, per 1,000 reports | 64 | 101 | 9 |
| Classified as injury | 86.2% | 74.6% | 36.2% |
| Classified as malfunction | 7.4% | 15.2% | 62.3% |
| Filed by the manufacturer | 100% | 99.6% | 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 NPT
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Edwards SAPIEN 3 Transcatheter Heart valve | 8,127 | 668 | 9.2% |
| Evolut R Transcatheter Aortic Valve | 6,444 | 521 | 9.6% |
| Evolut Pro Plus Valve | 5,873 | 780 | 12.8% |
| Evolut Fx Valve | 5,267 | 851 | 14.1% |
| Evolut Pro Transcatheter Aortic Valve | 3,668 | 422 | 11% |
| Edwards SAPIEN 3 Ultra Transcatheter Heart Valve | 3,737 | 714 | 14% |
| Evolut Fx Plus Valve | 3,448 | 2,316 | 8.9% |
| Edwards COMMANDER DELIVERY SYSTEM | 3,105 | 368 | 12.3% |
| Edwards SAPIEN 3 Ultra RESILIA Transcatheter Heart Valve | 2,885 | 1,128 | 11.6% |
| Evolut Fx Dcs | 2,570 | 860 | 10.8% |
| Edwards SAPIEN XT Transcatheter Heart Valve | 2,249 | 48 | 7.6% |
| SAPIEN 3 Transcatheter Heart Valve | 2,196 | 419 | 6% |
| Corevalve Transcatheter Aortic Valve | 1,669 | 60 | 9.6% |
| Edwards Sapien Transcatheter Heart Valve | 1,947 | 7 | 14.3% |
| Navitor Transcatheter Aortic Valve | 1,382 | 245 | 9% |
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 Navitor Vision reports
How many FDA reports name Navitor Vision?
2,045 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 1,258 in the latest 12 months.
What kinds of events are reported?
injury (86.2%), malfunction (7.4%) and death (6.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
perivalvular leak (16.2%), migration or expulsion of device (14.3%), difficult to fold, unfold or collapse (12.4%), improper or incorrect procedure or method (6.8%) and intravalvular regurgitation (4.1%). 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 Navitor Vision 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.