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Bard® Clean-Cath® Intermittent Catheter 421710Recalls & 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 00801741038808), received between Nov 11, 2020 and Nov 11, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Sharp Edges” (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

  • Sharp Edges1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionNov 11, 2020Sharp Edges; Sharp Edges

    IT WAS REPORTED THAT THE CATHETER ALLEGEDLY HAD A SHARP TIP THAT COULD CAUSE DAMAGE TO URETHRAL AND BLADDER TISSUES. PER ADDITIONAL INFORMATION RECEIVED VIA IBC ON 24OCT2020, NO ADVERSE EVENT OCCURRED, IT WAS JUST MENTIONED THAT THE REPORTED CONDITION HAS POTENTIAL FOR HARM, BUT NO HARM OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

    MAUDE report 10823271 ↗

Other CATHETER, UROLOGICAL devices

All CATHETER, UROLOGICAL devices →

Sources and updates

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