Bardex® Lubri-Sil® I.C. All-Silicone Foley Catheter 73024SIRecalls & reported problems
C. R. Bard, Inc. · Bardex® Lubri-Sil® I.C. All-Silicone Coated 30 cc 3 way Foley Catheter · Class 2
All models of Bardex Lubri-Sil I.C. All-Silicone Foley Catheter (26)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741025525), received between Sep 18, 2020 and Apr 15, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Puncture/Hole” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Material Puncture/Hole2
- Decrease in Pressure1
- Material Rupture1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 15, 2025Material Puncture/Hole; Material Puncture/Hole
IT WAS REPORTED CUSTOMER HAVING AN EXTREME ISSUE WITH ALL OUR 3-WAY FOLEY CATHETERS LEAKING WITH PIN HOLES AT THE BASE OF THE 3 WAYS. THE TWO THAT THEY HAD CURRENTLY WERE AND, THE TEAM SAID THAT THEY SINCE THIS HAPPENED, THEY TRY THEM OUT FIRST. THE TEAM SAID THEY WENT THROUGH AT LEAST 7 IN TWO DAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21840860 ↗MalfunctionApr 15, 2025Material Puncture/Hole; Material Puncture/Hole
IT WAS REPORTED THAT CUSTOMER HAD AN EXTREME ISSUE WITH ALL THEIR 3-WAY FOLEY CATHETERS LEAKING WITH PIN HOLES AT THE BASE OF THE 3 WAYS. THE TWO THAT THEY HAD CURRENTLY WERE 73024SI AND 70522SI, THE TEAM SAID THAT THEY SINCE THIS HAPPENED, THEY TRY THEM OUT FIRST. THE TEAM SAID THEY WENT THROUGH AT LEAST 7 IN TWO DAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21839790 ↗MalfunctionSep 18, 2020Decrease in Pressure; Material Rupture; Decrease in Pressure
IT WAS REPORTED THAT THE BALLOON ALLEGEDLY POPPED INSIDE THE PATIENT WHEN FILLED WITH ONLY 10CC WATER WHEN THE PACKAGE INSTRUCTS THE USE OF 30CC.
Patient problems: Insufficient Information; No Consequences Or Impact To Patient
MAUDE report 10555389 ↗
Other CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES devices
- Bardex® Lubri-Sil® I.C. Temperature-Sensing All-Silicone Foley Catheter 119314C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES1 recall3,889 reports
- Bardex® I.C. Foley Catheter 0165SI14C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES1,994 reports
- Bardex® I.C. Foley Catheter 0165SI16C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES1,052 reports
- Bardex® Lubri-Sil® I.C. All-Silicone Foley Catheter 1758SI14C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES778 reports
- Bardex® I.C. Temperature Sensing Foley Catheter 129414MC. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES436 reports
- Bardex® Lubri-Sil® I.C. All-Silicone Temp Sensing Foley Catheter 119316MC. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES231 reports
- Bardex® Lubri-Sil® I.C. Temperature-Sensing All-Silicone Foley Catheter 119316C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES198 reports
- Bardex® I.C. Foley Catheter 0165SI18C. R. Bard, Inc. · CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES181 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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