Angled Tip G14598Recalls & reported problems
Cook Incorporated · Angled Tip Ureteral Catheter with Bentson PTFE-Coated Wire Guide · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827002145986), received between Apr 27, 2017 and Apr 27, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Separation” (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 16, 2026.
Most reported problems
Device problems
- Material Separation2
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 27, 2017Material Separation; Material Separation
IT WAS REPORTED BY THE USER FACILITY THAT A PATIENT UNDERWENT A CHOLECYSTECTOMY LAPAROSCOPY WITH IOC PROCEDURE. THE SURGERY STAFF HAS REPORTED THAT THEY HAVE COME ACROSS A DEFECTIVE ANGLED TIP URETERAL CATHETER SET PRIOR TO PATIENT CONTACT. THE STAFF REPORTED THAT THE SMALL CAP ON THE END IS NOT ATTACHED AND JUST LOOSE IN THE PACKAGING. HOWEVER, THE PROCEDURE WAS COMPLETED WITH A DIFFERENT CATHETER AND NO ADDITIONAL PROCEDURES OR ADVERSE EFFECTS ON THE PATIENT WERE WARRANT DUE TO THIS OCCURRENCE. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6525783 ↗MalfunctionApr 27, 2017Material Separation; Material Separation
IT WAS REPORTED BY THE USER FACILITY THAT A PATIENT UNDERWENT A CHOLECYSTECTOMY LAPAROSCOPY WITH IOC PROCEDURE. THE SURGERY STAFF HAS REPORTED THAT THEY HAVE COME ACROSS A DEFECTIVE ANGLED TIP URETERAL CATHETER SET PRIOR TO PATIENT CONTACT. THE STAFF REPORTED THAT THE SMALL CAP ON THE END IS NOT ATTACHED AND IS ONLY LOOSE IN THE PACKAGING. HOWEVER, THE PROCEDURE WAS COMPLETED WITH A DIFFERENT CATHETER AND NO ADDITIONAL PROCEDURES OR ADVERSE EFFECTS TO THE PATIENT WERE WARRANT DUE TO THIS OCCURRENCE. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6525781 ↗
Other CATHETER, UROLOGICAL devices
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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