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Bardia® Coude Olive Tip Urethral Foley Catheter 802522Recalls & reported problems

C. R. Bard, Inc. · Bardia® Coude Olive Tip Urethral Catheter · Class 2

All models of Bardia Coude Olive Tip Urethral Foley Catheter (6)

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 00801741039089), received between Mar 12, 2020 and Mar 12, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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

  • Difficult to Insert1

Patient problems

  • No Known Impact Or Consequence To Patient1
  • Pain1

Recent adverse event reports

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

  • MalfunctionMar 12, 2020Difficult to Insert

    IT WAS REPORTED THAT THE PATIENT COULD ONLY GET THE CATHETER TO GO IN ABOUT AN INCH WHICH WAS PAINFUL. NO MEDICAL INTERVENTION WAS REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient; Pain

    MAUDE report 9825517 ↗

Other CATHETER, UROLOGICAL devices

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Sources and updates

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