Skip to content

Bardex® Lubricath® Foley Catheter Female Length 0169L18Recalls & reported problems

C. R. Bard, Inc. · Bardex® Lubricath® 5cc Balloon Female Length Foley Catheter Lubricious Coated · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741018015), received between Sep 10, 2021 and Sep 10, 2021 — 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

Device problems

  • Incorrect Measurement1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 10, 2021Incorrect Measurement; Incorrect Measurement

    IT WAS REPORTED THAT THE FOLEY CATHETERS WERE TOO SHORT AND PATIENT NEED LONGER. THE PATIENT HAD BEEN USING THIS PRODUCT FOR MORE THAN 90 DAYS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12453444 ↗

Other CATHETER, COUDE devices

All CATHETER, COUDE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page