Bard® Polyurethane Ureteral Catheters, Open Tip 135005Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801741126946), received between Dec 21, 2023 and Dec 21, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (1 report).

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 21, 2023Deformation Due to Compressive Stress; Deformation Due to Compressive Stress

  IT WAS REPORTED THAT DURING CYSTOSCOPY PROCEDURE, DOCTOR NOTICED A DEFECTIVE AREA OF THREE OF THE RED, RIGHT SIDED, 5FR X69CM OPEN TIP URETHRAL CATHETERS. ALL FROM THE SAME LOT NUMBER. THEY EXPLAINED THAT THE END OF THE CATHETER WITH THE SCREW CAP ATTACHMENT WAS CRIMPED AND COULD NOT ATTACH GUIDE WIRE TO PASS THROUGH. ALSO STATED THERE WAS DELAY OF PROCEDURE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 18376964 ↗