Bard® Polyurethane Ureteral Catheters, Open Tip 134005Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801741126892), received between Jul 26, 2024 and Jul 26, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect Measurement” (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.

• MalfunctionJul 26, 2024Incorrect Measurement; Incorrect Measurement

  IT WAS REPORTED THAT CUSTOMER ORDERED PRODUCT THAT WAS LISTED AS A 5FR OPEN TIP URETHRAL CATHETER IN REPLACE OF 139005 BEING ON BO. WHEN CUSTOMER RECEIVED PRODUCT, A WIRE WOULD NOT PASS THROUGH, THE CATHETER WAS TOO SMALL, WHICH IT SHOULD NOT HAVE BEEN. CUSTOMER CANNOT USE THIS ITEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19837728 ↗