Bard® Woven Ureteral Catheter 036106Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741073397), received between May 26, 2017 and Jun 1, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Component Missing” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 1, 2017Component Missing

  IT WAS REPORTED THAT THE CATHETER WAS MISSING FROM THE SEALED PACKAGING.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6604322 ↗
• MalfunctionMay 26, 2017Component Missing; Out-Of-Box Failure

  IT WAS REPORTED THAT THE CATHETER WAS MISSING FROM THE PACKAGING. THE COMPLAINANT STATED THAT THE PACKAGING WAS SEALED , WHEN IT WAS NOTED THAT NO CATHETER WAS INSIDE. NO PATIENT INVOLVEMENT WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6595510 ↗