Bard® InLay® Ureteral Stent with HydroGlide™ Guidewire 777724Recalls & reported problems
C. R. Bard, Inc. · INLAY URETERAL STENT W/HYDROGLIDE GUIDEWIRE · Class 2 · Implant
All models of Bard InLay Ureteral Stent with HydroGlide Guidewire (17)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10801741014618), received between Feb 13, 2018 and Jul 12, 2024 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- Material Fragmentation2
- Component Misassembled1
- Component Missing1
- Device Damaged Prior to Use1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Patient Involvement2
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 12, 2024Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT THE DJ TUBE OF THE URETERAL STENT WAS BROKEN BEFORE USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19729051 ↗MalfunctionApr 6, 2022Component Misassembled; Component Misassembled
IT WAS REPORTED THAT THE SUTURE WAS NOT ATTACHED TO THE STENT WHEN NURSE OPENED THE PACKAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14020843 ↗MalfunctionDec 30, 2021Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT THE URETERAL STENT WAS BROKEN THE COIL SEPARATING FROM THE STRAIGHT SITE UPON OPENING THE PACKAGE. IT WAS MENTIONED THAT A NEW URETERAL STENT HAD BEEN UNPACKED FOR USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13120941 ↗MalfunctionMay 12, 2021Component Missing; Component Missing
IT WAS REPORTED THAT AFTER OPENING THE PACKAGE, THE GUIDE WIRE WAS FOUND BUT NO STENT WAS FOUND INSIDE THE PACKAGE. A NEW ONE HAD BEEN UNPACKED TO USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11815890 ↗MalfunctionFeb 27, 2018Break
IT WAS REPORTED THAT THE STENT WAS FOUND BROKEN PRIOR TO USE.
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 7300486 ↗MalfunctionFeb 13, 2018Break; Device Damaged Prior to Use
IT WAS REPORTED THAT THE DEVICE BROKEN PRIOR TO USE.
Patient problems: No Patient Involvement
MAUDE report 7267120 ↗
Other STENT, URETERAL devices
- Bard® InLay Optima® Ureteral Stent 788426C. R. Bard, Inc. · STENT, URETERAL1 recall100 reports
- Bard® InLay Optima® Ureteral Stent 788626C. R. Bard, Inc. · STENT, URETERAL122 reports
- Bard® InLay® Ureteral Stent with HydroGlide™ Guidewire 777626C. R. Bard, Inc. · STENT, URETERAL118 reports
- Bard® InLay® Ureteral Stent with HydroGlide™ Guidewire 777426C. R. Bard, Inc. · STENT, URETERAL108 reports
- Bard® InLay® Ureteral Stent 778626C. R. Bard, Inc. · STENT, URETERAL100 reports
- Percuflex™ Plus M0061752530Boston Scientific Corporation · STENT, URETERAL1 death99 reports
- Contour VL™ M0061801560Boston Scientific Corporation · STENT, URETERAL1 recall45 reports
- Polaris™ Ultra M0061921330Boston Scientific Corporation · STENT, URETERAL71 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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