Bard® TigerTail™ Flexible Tip Ureteral Catheters 139006Recalls & reported problems
C. R. Bard, Inc. · Bard® TigerTail™ Flexible Tip Ureteral Catheters · Class 2
All models of Bard TigerTail Flexible Tip Ureteral Catheters (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10801741127103), received between Apr 11, 2022 and Mar 3, 2026 — classified as 1 injury, 5 malfunctions.
The most frequently reported specific device problem is “Material Too Rigid or Stiff” (4 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
- Material Too Rigid or Stiff4
- Material Fragmentation2
- Separation Failure2
- Nonstandard Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Foreign Body In Patient1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryMar 3, 2026Material Fragmentation
IT WAS REPORTED THAT THE PART OF THE BARD POLYURETHANS URETERAL CATHETER CAME OFF INSIDE THE PATIENT AS THE DEVICE FAILED (E.G. BROKE, COULDN'T GET IT TO WORK OR STOPPED WORKING). IT WAS SEEN ON X-RAY AND TAKEN OUT BY THE SURGEON.
Patient problems: Foreign Body In Patient
MAUDE report 24502116 ↗MalfunctionNov 6, 2023Material Too Rigid or Stiff; Separation Failure; Material Too Rigid or Stiff; Separation Failure
IT WAS REPORTED THAT THE EVEN AFTER LOOSENING THE CATHETER CONNECTOR, URETERAL CATHETER DID NOT SLIDE OR WAS STUCK. THERE WAS SOMETHING MOVING, BUT THE CATHETER WAS STRETCHED TOO MUCH. IT WAS STATED THAT THE CONNECTOR OF THE URETERAL CATHETER WAS HARD TO OPERATE (LOT#MYHN3050), (LOT#MYHP1895), (LOT#MYHT337).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18074230 ↗MalfunctionNov 3, 2023Material Too Rigid or Stiff; Separation Failure; Material Too Rigid or Stiff; Separation Failure
IT WAS REPORTED THAT THE EVEN AFTER LOOSENING THE CATHETER CONNECTOR, URETERAL CATHETER DID NOT SLIDE OR WAS STUCK. THERE WAS SOMETHING MOVING, BUT THE CATHETER WAS STRETCHED TOO MUCH. IT WAS STATED THAT THE CONNECTOR OF THE URETERAL CATHETER WAS HARD TO OPERATE (LOT#MYHN3050, LOT#MYHP1895, LOT#MYHT337).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18066502 ↗MalfunctionNov 2, 2023Nonstandard Device; Material Too Rigid or Stiff; Nonstandard Device; Material Too Rigid or Stiff
IT WAS REPORTED THAT EVEN AFTER LOOSENING THE CATHETER CONNECTOR, URETERAL CATHETER DID NOT SLIDE OR WAS STUCK. THERE WAS SOMETHING MOVING, BUT THE CATHETER WAS STRETCHED TOO MUCH. IT WAS STATED THAT THE CONNECTOR OF THE URETERAL CATHETER WAS HARD TO OPERATE (LOT# MYHN3050, LOT# MYHP1895, LOT# MYHT337).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18055338 ↗MalfunctionJul 1, 2022Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT THE FLEXIBLE TIP TIGER TAIL CATHETER WOULD NOT THREAD THROUGH THE CYSTO SHEATH. UPON TROUBLESHOOTING THE PROBLEM, THE TIGER TAIL SNAPPED IN HALF AND BOTH PIECES WERE INTACT AND REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14888058 ↗MalfunctionApr 11, 2022Material Too Rigid or Stiff; Material Too Rigid or Stiff
IT WAS REPORTED THAT THE DOCTOR USED THE TIGER TAIL URETERAL CATHETER AT THE END OF THE URETEROSCOPY SURGERY, BUT UNFORTUNATELY BLOOD CAME OUT FROM THE PATIENT AT THE END. THE FEEDBACK FROM THE DOCTOR UPON THE INCIDENT WAS THAT THE CATHETER WAS STIFF. THE PATIENT EXPERIENCED MINOR BLEEDING. NO MEDICAL INTERVENTION WAS REPORTED.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 14078778 ↗
Other CATHETER, UROLOGICAL devices
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50614C. R. Bard, Inc. · CATHETER, UROLOGICAL883 reports
- Magic3™ Intermittent Catheter with Sure-Grip™ Sleeve 53614GC. R. Bard, Inc. · CATHETER, UROLOGICAL692 reports
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50616C. R. Bard, Inc. · CATHETER, UROLOGICAL2 deaths443 reports
- GENTLECATH GLIDE 421567Convatec, Purchasing Department · Catheter, Urological342 reports
- Magic3™ Intermittent Catheter with Sure-Grip™ Sleeve 53616GC. R. Bard, Inc. · CATHETER, UROLOGICAL301 reports
- Bardex® Foley Catheter Silicone Coated 0167V22SC. R. Bard, Inc. · CATHETER, UROLOGICAL187 reports
- Bardex® Foley Catheter Silicone Coated 0167V20SC. R. Bard, Inc. · CATHETER, UROLOGICAL175 reports
- Bardia® Coude Olive Tip Urethral Foley Catheter 802516C. R. Bard, Inc. · CATHETER, UROLOGICAL170 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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