Extension Tube 6A4194Recalls & reported problems
C. R. Bard, Inc. · Latex Extension Tube, 9/32" I.D. x 18" with Connector · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00801741051579), received between May 9, 2018 and Mar 21, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Restricted Flow rate” (3 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
- Restricted Flow rate3
- Backflow1
- Component Missing1
- Device Operational Issue1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Consequences Or Impact To Patient2
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 21, 2025Restricted Flow rate; Restricted Flow rate
IT WAS REPORTED THAT LEG BAGS WERE NOT OPENING TO COLLECT URINE AS THEY SHOULD BE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21662645 ↗MalfunctionAug 22, 2024Restricted Flow rate; Restricted Flow rate
IT WAS REPORTED THAT THE CONNECTOR ON EXTENSION TUBING WOULD NOT ALLOW THE URINE TO FLOW AND HAD WASTED 3 CATHETERS SO FAR DUE TO THAT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20030444 ↗MalfunctionSep 6, 2022Component Missing; Component Missing
IT WAS REPORTED THAT THE CUSTOMER RECEIVED THE ORDER AND IT ONLY CONTAINED A TUBING AND THERE WERE NO CONNECTORS ON THE END.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15361684 ↗MalfunctionAug 15, 2019Backflow; Material Twisted/Bent
IT WAS REPORTED THAT THE EXTENSION TUBING TENDS TO BEND AND AS A RESULT URINE BACKS UP. NO MEDICAL INTERVENTION WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8898954 ↗MalfunctionMay 9, 2018Restricted Flow rate; Restricted Flow rate; Device Operational Issue
IT WAS REPORTED THAT THE URINE WAS BACKING UP IN THE EXTENSION TUBING.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 7499790 ↗
Other COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER devices
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- SureStep™ Foley Tray System Complete Care® Add-A-Foley Catheter A399400AC. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER2 recalls0 reports
- Bard® Urinary Drainage Bag 153509C. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER91 reports
- Bard® Urinary Drainage Bag 153504C. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER89 reports
- SureStep™ Foley Tray System Complete Care® Add-A-Foley Catheter A304400AC. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER1 recall12 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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