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Bard® Urethral Catheterization Tray with Red Rubber Catheter 774415Recalls & reported problems

C. R. Bard, Inc. · Bard® Urethral Catheterization Tray with Red Rubber Catheter · Class 2

All models of Bard Urethral Catheterization Tray with Red Rubber Catheter (4)

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 00801741040221), received between Feb 6, 2018 and Feb 6, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

  • Component Missing1

Patient problems

  • 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 6, 2018Component Missing

    IT WAS REPORTED THAT THE CATHETER WAS MISSING THE DRAINAGE EYES, WHICH PREVENTED THE URINE FROM DRAINING. THE DEVICE WAS REPLACED AND NO MEDICAL INTERVENTION WAS REQUIRED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7244331 ↗

Other CATHETER, URETERAL, GASTRO-UROLOGY devices

All CATHETER, URETERAL, GASTRO-UROLOGY devices →

Sources and updates

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