Device brand name · Snare flexible
Ultratome XL: medical device reports filed with FDA
411 reports name it, 2005–2026. Manufacturer given most often on reports: Boston Scientific. Product code FDI.
- 411
- device reports naming the brand
- 0% of all MAUDE reports · about 20 a year
- 38
- reports, 12 months to August 2026
- 66 in the 12 months before
- 97.3%
- classified as malfunction
- 86.4% across the product code
- 0.5%
- classified as death, as reported
- 2 reports · not verified by FDA
FDA's MAUDE database holds 411 reports that name the brand "Ultratome XL" (snare flexible), received between July 2005 and August 2026; the manufacturer given most often on reports is Boston Scientific. Spellings of one product vary from report to report.
38 reports arrived in the 12 months to August 2026, down 42% from 66 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 (97.3%), injury (2.2%) and death (0.5%); across all snare, flexible reports (product code FDI) death is recorded in 0.2% and malfunction in 86.4%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are break (65.7%), positioning problem (12.4%) and material deformation (11.9%). The patient problems coded most often are hemorrhage/blood loss/bleeding, pancreatitis and cholangitis. 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 4,658 reports carrying product code FDI. 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 |
|---|---|---|---|
| Breakthe device broke | 270 | 65.7% | 15.3% |
| Positioning problem | 51 | 12.4% | 1.9% |
| Material deformation | 49 | 11.9% | 1.4% |
| Device dislodged or dislocated | 15 | 3.6% | 0.3% |
| Deformation due to compressive stress | 14 | 3.4% | 0.4% |
| Failure to fold | 12 | 2.9% | 0.2% |
| Difficult to advance | 11 | 2.7% | 0.3% |
| Failure to align | 11 | 2.7% | 0.3% |
| Device contaminated during manufacture or shipping | 10 | 2.4% | 0.3% |
| Material split, cut or torn | 8 | 1.9% | 0.4% |
| Failure to conduct | 6 | 1.5% | 1.1% |
| Material twisted/bent | 6 | 1.5% | 1.5% |
| Material integrity problema problem with the device material | 5 | 1.2% | 0.1% |
| Defective devicethe device was defective | 4 | 1% | 1% |
| Kinkedthe tube or line kinked | 4 | 1% | 0.4% |
| Melted | 3 | 0.7% | 0.5% |
| Bent | 2 | 0.5% | 0.8% |
| Crackthe device cracked | 2 | 0.5% | 0% |
| Difficult to removethe device was hard to remove | 2 | 0.5% | 1.5% |
| Detachment of device or device componentpart of the device came off | 1 | 0.2% | 3.4% |
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 |
|---|---|---|
| Hemorrhage/blood loss/bleeding | 6 | 1.5% |
| Pancreatitisinflammation of the pancreas | 4 | 1% |
| Cholangitis | 2 | 0.5% |
| Perforation | 2 | 0.5% |
| Foreign body in patientpart of a device left in the patient | 1 | 0.2% |
| Inflammationinflammation | 1 | 0.2% |
| Myocarditisinflammation of the heart muscle | 1 | 0.2% |
| No patient involvement | 1 | 0.2% |
| Sepsisa severe body-wide response to infection | 1 | 0.2% |
| Swelling/ edema | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Ultratome XL | Product code FDI | All MAUDE reports |
|---|---|---|---|
| Reports | 411 | 4,658 | 26,136,888 |
| Share of that pool | — | 8.8% | 0% |
| Classified as death, per 1,000 reports | 5 | 2 | 9 |
| Classified as injury | 2.2% | 12.8% | 36.2% |
| Classified as malfunction | 97.3% | 86.4% | 62.3% |
| Filed by the manufacturer | 99.5% | 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 FDI
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| SENSATION Short Throw | 733 | 83 | 0% |
| Captivator | 510 | 29 | 0% |
| Rotatable Snare | 486 | 20 | 0% |
| Captiflex | 400 | 13 | 0% |
| ACUSNARE Polypectomy Snare | 319 | 13 | 0% |
| Hydratome Rx Sphincterotome | 458 | 0 | 0.2% |
| Boston Scientific | 580 | 5 | 3.3% |
| Fresenius | 314 | 0 | 6.1% |
| NCircle Tipless Stone Extractor | 1,463 | 232 | 0% |
| Prisma Control Unit | 566 | 0 | 6% |
| Conmed | 900 | 89 | 0.2% |
| Optiflux 180nre Dialyzer Finished Assy | 3,373 | 69 | 0.6% |
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 Ultratome XL reports
How many FDA reports name Ultratome XL?
411 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 38 in the latest 12 months.
What kinds of events are reported?
malfunction (97.3%), injury (2.2%) and death (0.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
break (65.7%), positioning problem (12.4%), material deformation (11.9%), device dislodged or dislocated (3.6%) and deformation due to compressive stress (3.4%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.5%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Ultratome XL 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.