Bardex® Lubricath® Foley Catheter Emmett Model 0138L24Recalls & reported problems
C. R. Bard, Inc. · Bardex® Lubricath® Emmett Model Foley Catheter Three Eyes Long Length Round Tip 3 Way Continuous Irrigation 30cc Balloon Lubricious Coated · 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 00801741018862), received between Nov 22, 2024 and Nov 22, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Inaccurate Flow Rate” (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.
Reports received per month
Most reported problems
Device problems
- Inaccurate Flow Rate1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 22, 2024Inaccurate Flow Rate; Inaccurate Flow Rate
IT WAS REPORTED THAT THE URINE FLOWS FROM THE 3RD CHANNEL PORT TIP AND THE DRAINAGE CHANEL WAS CONNECTED TO THE URINARY BAG FOR DRAINING, BUT THE URINE GOES TO BOTH THESE 2 CHANNELS WHICH WAS NOT SUPPOSED TO. PER ADDITIONAL INFORMATION RECEIVED VIA MAIL ON 23DEC2024, STATED THAT THE URINE WAS LEAKING FROM THE 3RD LUMEN WHICH WAS SUPPOSED TO USE FOR IRRIGATION ONLY AND THEY PUT A LABOR BAND ON THE CATHETER TIP TO KINK AND PREVENT THE LEAKAGE. PER CLARIFICATION MAIL RECEIVED FROM UCC ON 30DEC2024, STATED THAT THE PATIENT HAD ISSUES WITH 2 MATERIAL# (MATERIAL#0138L24 AND MATERIAL#0167L24).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20759496 ↗
Other CATHETER, UROLOGICAL devices
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50614C. R. Bard, Inc. · CATHETER, UROLOGICAL883 reports
- Magic3™ Intermittent Catheter with Sure-Grip™ Sleeve 53614GC. R. Bard, Inc. · CATHETER, UROLOGICAL692 reports
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50616C. R. Bard, Inc. · CATHETER, UROLOGICAL2 deaths443 reports
- GENTLECATH GLIDE 421567Convatec, Purchasing Department · Catheter, Urological342 reports
- Magic3™ Intermittent Catheter with Sure-Grip™ Sleeve 53616GC. R. Bard, Inc. · CATHETER, UROLOGICAL301 reports
- Bardex® Foley Catheter Silicone Coated 0167V22SC. R. Bard, Inc. · CATHETER, UROLOGICAL187 reports
- Bardex® Foley Catheter Silicone Coated 0167V20SC. R. Bard, Inc. · CATHETER, UROLOGICAL175 reports
- Bardia® Coude Olive Tip Urethral Foley Catheter 802516C. R. Bard, Inc. · CATHETER, UROLOGICAL170 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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