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Bard® Foley Catheter Silicone Coated 266716Recalls & reported problems

C. R. Bard, Inc. · Bard®Foley Catheter, Silicone Coated, 30cc Balloon · Class 2

All models of Bard Foley Catheter Silicone Coated (10)

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 00801741039690), received between Nov 21, 2019 and Nov 21, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Burst Container or Vessel” (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

  • Burst Container or Vessel1

Patient problems

  • 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 21, 2019Burst Container or Vessel; Burst Container or Vessel

    IT WAS REPORTED THAT 3 BALLOONS BURSTS WHEN INFLATED WITH 30 CCS OF SALINE. NO MEDICAL INTERVENTION WAS REQUIRED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9356306 ↗

Other CATHETER, UROLOGICAL devices

All CATHETER, UROLOGICAL devices →

Sources and updates

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