Bard® Pediatric Urine Meter 153206Recalls & reported problems
C. R. Bard, Inc. · Bard® Pediatric Urine Meter · 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 00801741033124), received between May 24, 2024 and May 24, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Restricted 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
- Restricted 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.
MalfunctionMay 24, 2024Restricted Flow rate; Restricted Flow rate
IT WAS REPORTED THAT PATIENT HAD INDWELLING FOLEY CATHETER IN PLACE CONNECTED TO BARD URINARY BURETROL DRAIN. EACH TIME NURSES WERE EMPTYING THE BURETROL CHAMBER THERE WAS ONLY 10-30ML IN IT EVEN AFTER GIVING LASIX FOR INCREASED EDEMA, THE URINE OUTPUT WAS ALWAYS THE SAME. NURSE NOTICED URINE WOULD STOP DRAINING AROUND 10-15ML BUT STILL HAVE URINE IN THE TUBING. AFTER MANIPULATING THE TUBING AND OPENED THE END OF THE BURETROL TO FREE FLOW INTO A STERILE CUP FOR SEVERAL MINUTES, DID THE URINE OUTPUT INCREASE TO 188ML OUT. FOLEY CATHETER WAS ALWAYS PATENT, BUT THE DRAINAGE DEVICE WOULD NOT ALLOW URINE TO FLOW AFTER IT WOULD FILL TO THE 10-30ML MARK. URINARY BURETROL DRAIN WAS DISCONNECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19392555 ↗
Other COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER devices
- Bardia® Closed System Urinary Drainage Bag With Anti-Reflux Chamber 802001C. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER117 reports
- Bard® Urine Meter with Bag 153214AC. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER107 reports
- Bard® Urinary Drainage Bag with Anti-Reflux Chamber 154002C. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER107 reports
- Bard® Urine Meter with Bag 153204C. R. Bard, Inc. · COLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER106 reports
- 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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