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Bard® Foley Tray With Bardex® Lubricath® Foley Catheter 947616Recalls & reported problems

C. R. Bard, Inc. · Bard® Foley Tray With Bardex® Lubricath® Foley Catheter · 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 00801741024788), received between Oct 3, 2018 and Oct 3, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Infuse” (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

  • Failure to Infuse1
  • Inflation Problem1

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.

  • MalfunctionOct 3, 2018Inflation Problem; Failure to Infuse; Failure to Infuse

    IT WAS REPORTED THAT THE FOLEY CATHETER BALLOON WOULD NOT INFLATE. NO MEDICAL INTERVENTION WAS REQUIRED.

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

    MAUDE report 7930150 ↗

Other CATHETER, COUDE devices

All CATHETER, COUDE devices →

Sources and updates

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