Devices › Drug eluting permanent right ventricular (rv) or right atrial (ra) pacemaker electrodes
Device brand name · No match
UltiPace Lead, 58cm MRI: medical device reports filed with FDA
764 reports name it, 2024–2026. Manufacturer given most often on reports: St Jude Medical Crm-Sylmar. Product code NVN.
- 764
- device reports naming the brand
- 0% of all MAUDE reports · about 306 a year
- 427
- reports, 12 months to August 2026
- 302 in the 12 months before
- 40.3%
- classified as malfunction
- 41.6% across the product code
- 1.2%
- classified as death, as reported
- 9 reports · not verified by FDA
764 medical device reports received by FDA name the brand "UltiPace Lead, 58cm MRI" (no match); the manufacturer given most often on reports is St Jude Medical Crm-Sylmar; received from January 2024 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
427 reports arrived in the 12 months to August 2026, up 41% from 302 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 (58.5%), malfunction (40.3%) and death (1.2%); across all drug eluting permanent right ventricular (rv) or right atrial (ra) pacemaker electrodes reports (product code NVN) death is recorded in 2.2% and malfunction in 41.6%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are device dislodged or dislocated (33.1%), failure to capture (25.4%) and capturing problem (15.8%). The patient problems coded most often are cardiac perforation, arrhythmia and discomfort. 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 229,796 reports carrying product code NVN. 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 |
|---|---|---|---|
| Device dislodged or dislocated | 253 | 33.1% | 15.8% |
| Failure to capture | 194 | 25.4% | 12.6% |
| Capturing problem | 121 | 15.8% | 4.7% |
| Difficult to fold, unfold or collapse | 106 | 13.9% | 1.1% |
| Device sensing problem | 73 | 9.6% | 3.7% |
| Breakthe device broke | 67 | 8.8% | 5.2% |
| High impedance | 54 | 7.1% | 9.1% |
| Retraction problem | 51 | 6.7% | 0.7% |
| Over-sensing | 32 | 4.2% | 17.9% |
| Low impedance | 29 | 3.8% | 5.1% |
| Material twisted/bent | 29 | 3.8% | 0.5% |
| Failure to sense | 25 | 3.3% | 2% |
| Under-sensing | 23 | 3% | 4.5% |
| Intermittent capture | 20 | 2.6% | 1.1% |
| Insufficient device problem information | 17 | 2.2% | 2.6% |
| Therapy delivered to incorrect body area | 15 | 2% | 0.3% |
| Failure to advance | 10 | 1.3% | 0.3% |
| Signal artifact/noise | 9 | 1.2% | 9% |
| Contamination of device ingredient or reagent | 6 | 0.8% | 0.1% |
| Difficult to removethe device was hard to remove | 6 | 0.8% | 0.4% |
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 |
|---|---|---|
| Cardiac perforation | 44 | 5.8% |
| Arrhythmia | 43 | 5.6% |
| Discomfortdiscomfort | 24 | 3.1% |
| Syncope/fainting | 14 | 1.8% |
| Pericardial effusionfluid around the heart | 12 | 1.6% |
| Dizzinesslight-headedness or unsteadiness | 11 | 1.4% |
| Fever | 5 | 0.7% |
| Low blood pressure/ hypotension | 5 | 0.7% |
| Valvular insufficiency/ regurgitation | 5 | 0.7% |
| Dyspneashortness of breath | 3 | 0.4% |
| Fatiguetiredness | 2 | 0.3% |
| Heart failure/congestive heart failure | 2 | 0.3% |
| Hematomaa collection of blood under the skin or in tissue | 2 | 0.3% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 1 | 0.1% |
| Cardiac tamponade | 1 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | UltiPace Lead, 58cm MRI | Product code NVN | All MAUDE reports |
|---|---|---|---|
| Reports | 764 | 229,796 | 26,136,888 |
| Share of that pool | — | 0.3% | 0% |
| Classified as death, per 1,000 reports | 12 | 22 | 9 |
| Classified as injury | 58.5% | 56.2% | 36.2% |
| Classified as malfunction | 40.3% | 41.6% | 62.3% |
| Filed by the manufacturer | 100% | 96.9% | 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 NVN
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Tendril Sts | 54,036 | 4,320 | 3.1% |
| SelectSecure MRI SureScan | 20,961 | 4,994 | 1.3% |
| Tendril St | 20,156 | 547 | 5.2% |
| Ingevity Mri | 17,101 | 1,749 | 0.3% |
| Ingevity+ | 15,340 | 2,150 | 0.3% |
| Tendril Sdx Lead | 9,380 | 431 | 4.5% |
| CapSure Fix MRI | 5,755 | 600 | 0.6% |
| Solia S 53 | 4,997 | 647 | 0.5% |
| Tendril Mri | 7,076 | 422 | 4.1% |
| Drug Eluting Permanent Right Ventricular Rv Or Right Atrial Ra Pacemaker Ele | 4,462 | 405 | 0.3% |
| Capsurefix Mri Surescan | 4,247 | 0 | 2.8% |
| Tendril Sdx | 8,316 | 3 | 2.3% |
| Ingevity | 9,039 | 299 | 0.9% |
| Ingevity + | 3,053 | 2,281 | 0.6% |
| Dextrus 4136 | 5,698 | 0 | 0.8% |
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 UltiPace Lead, 58cm MRI reports
How many FDA reports name UltiPace Lead, 58cm MRI?
764 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 427 in the latest 12 months.
What kinds of events are reported?
injury (58.5%), malfunction (40.3%) and death (1.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device dislodged or dislocated (33.1%), failure to capture (25.4%), capturing problem (15.8%), difficult to fold, unfold or collapse (13.9%) and device sensing problem (9.6%). 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 UltiPace Lead, 58cm MRI 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.