Bard® Woven Ureteral Catheter 038008Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741073595), received between Dec 27, 2023 and Dec 27, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fitting Problem” (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 27, 2023Fitting Problem; Fitting Problem

  IT WAS REPORTED THAT THE WHILE ATTEMPTING TO INJECT DYE INTO CONE TIP CATHETER, THE SYRINGE WAS NOT ABLE TO CONNECT. THE DOCTOR INFORMED THE ADAPTER NEEDS TO BE ORDERED. REPRESENTATIVE ADVISED THE CONE TIP NOR OLIVE TIP URETERAL CATHETER ARE SOLD WITH AN ADAPTER. PROVIDED PLASTIC ADAPTER PRODUCT NUMBER (140000).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18400187 ↗