Device brand name · Ureteral stent
Bard InLay Ureteral Stent with HydroGlide Guidewire: medical device reports filed with FDA
342 reports name it, 2017–2026. Manufacturer given most often on reports: C R Bard Covington -1018233. Product code FAD.
- 342
- device reports naming the brand
- 0% of all MAUDE reports · about 37 a year
- 17
- reports, 12 months to August 2026
- 44 in the 12 months before
- 86.5%
- classified as malfunction
- 70.6% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 342 reports that name the brand "Bard InLay Ureteral Stent with HydroGlide Guidewire" (ureteral stent), received between May 2017 and July 2026; the manufacturer given most often on reports is C R Bard Covington -1018233. Spellings of one product vary from report to report.
17 reports arrived in the 12 months to August 2026, down 61% from 44 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 (86.5%) and injury (13.5%); across all stent, ureteral reports (product code FAD) death is recorded in 0.2% and malfunction in 70.6%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are material fragmentation (43.3%), break (9.9%) and wrong label (7.3%). The patient problems coded most often are no patient involvement, appropriate clinical signs, symptoms and conditions term/code not available and pain. 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 5,909 reports carrying product code FAD. 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 |
|---|---|---|---|
| Material fragmentation | 148 | 43.3% | 10.1% |
| Breakthe device broke | 34 | 9.9% | 24.1% |
| Wrong label | 25 | 7.3% | 0.9% |
| Calcified | 21 | 6.1% | 8% |
| Biocompatibility | 20 | 5.8% | 1.7% |
| Patient device interaction problem | 15 | 4.4% | 2.2% |
| Accessory incompatible | 14 | 4.1% | 0.7% |
| Difficult to insertthe device was hard to insert | 10 | 2.9% | 0.9% |
| Component missing | 8 | 2.3% | 0.7% |
| Device damaged prior to usethe device was damaged before use | 6 | 1.8% | 1.3% |
| Fracturea broken bone | 5 | 1.5% | 2.1% |
| Tear, rip or hole in device packaging | 5 | 1.5% | 0.6% |
| Material split, cut or torn | 4 | 1.2% | 3.9% |
| Component misassembled | 3 | 0.9% | 0.3% |
| Device contamination with chemical or other material | 3 | 0.9% | 0.6% |
| Difficult to removethe device was hard to remove | 3 | 0.9% | 6.8% |
| Flaked | 3 | 0.9% | 0.3% |
| Partial blockage | 3 | 0.9% | 0.7% |
| Crackthe device cracked | 2 | 0.6% | 0.7% |
| Device dislodged or dislocated | 2 | 0.6% | 0.8% |
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 |
|---|---|---|
| No patient involvement | 44 | 12.9% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 36 | 10.5% |
| Painpain, site not specified | 15 | 4.4% |
| Discomfortdiscomfort | 8 | 2.3% |
| Foreign body in patientpart of a device left in the patient | 8 | 2.3% |
| Dysuriapain on passing urine | 7 | 2% |
| Urinary frequency / polyuria | 7 | 2% |
| Exposure to body fluids | 6 | 1.8% |
| Hematuria | 6 | 1.8% |
| Micturition urgency | 3 | 0.9% |
| Abdominal painstomach or belly pain | 2 | 0.6% |
| Dyspneashortness of breath | 2 | 0.6% |
| Skin discoloration | 2 | 0.6% |
| Swelling/ edema | 2 | 0.6% |
| Tachycardiafast heart rate | 2 | 0.6% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Bard InLay Ureteral Stent with HydroGlide Guidewire | Product code FAD | All MAUDE reports |
|---|---|---|---|
| Reports | 342 | 5,909 | 26,136,888 |
| Share of that pool | — | 5.8% | 0% |
| Classified as death, per 1,000 reports | 0 | 2 | 9 |
| Classified as injury | 13.5% | 28.5% | 36.2% |
| Classified as malfunction | 86.5% | 70.6% | 62.3% |
| Filed by the manufacturer | 100% | 94.5% | 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 FAD
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Polaris? Ultra | 478 | 49 | 0% |
| Bard InLay Optima Ureteral Stent | 394 | 44 | 0% |
| Percuflex Plus | 458 | 50 | 0.4% |
| Resonance Stent Set | 256 | 16 | 1.2% |
| Bard InLay Ureteral Stent | 232 | 25 | 0% |
| Filiform Double Pigtail Ureteral Stent Set | 227 | 38 | 0.4% |
| Bard InLay Optima Ureteral Stent with HydroGlide Guidewire | 220 | 14 | 0% |
| Universa Soft Ureteral Stent Set | 205 | 14 | 0% |
| Universa Firm Ureteral Stent Set | 203 | 12 | 0% |
| Contour | 2,235 | 38 | 0% |
| Polaris? Loop | 154 | 25 | 0.6% |
| Flexima? | 257 | 10 | 0.4% |
| Boston Scientific | 580 | 5 | 3.3% |
| Cotton-Leung Biliary Stent | 271 | 20 | 1.1% |
| Cook | 271 | 6 | 2.2% |
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 Bard InLay Ureteral Stent with HydroGlide Guidewire reports
How many FDA reports name Bard InLay Ureteral Stent with HydroGlide Guidewire?
342 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 17 in the latest 12 months.
What kinds of events are reported?
malfunction (86.5%) and injury (13.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
material fragmentation (43.3%), break (9.9%), wrong label (7.3%), calcified (6.1%) and biocompatibility (5.8%). 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 Bard InLay Ureteral Stent with HydroGlide Guidewire 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.