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Bard® Clean-Cath® Intermittent Catheter 421718Recalls & reported problems

C. R. Bard, Inc. · Bard® Clean-Cath® Intermittent Catheter · Class 2

All models of Bard Clean-Cath Intermittent Catheter (15)

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 00801741038846), received between Feb 5, 2020 and Feb 5, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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

  • Inadequacy of Device Shape and/or Size1
  • Incorrect Measurement1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionFeb 5, 2020Incorrect Measurement; Inadequacy of Device Shape and/or Size; Incorrect Measurement

    IT WAS REPORTED THAT THE DIAMETER OF THE 18FR CATHETER WAS SMALLER THAN WHAT THE PATIENT WAS USED TO RECEIVING.

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

    MAUDE report 9671899 ↗

Other CATHETER, UROLOGICAL devices

All CATHETER, UROLOGICAL devices →

Sources and updates

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