Bard® Weber Rectal Catheter 0006580Recalls & reported problems
C. R. Bard, Inc. · Bard® Weber Rectal Catheter · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10801741122177), received between May 11, 2017 and Nov 27, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Component Missing” (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
- Component Missing1
- Failure to Infuse1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 27, 2023Component Missing; Component Missing
IT WAS REPORTED THAT CUSTOMER WOULD LIKE TO KNOW WHY A BULB INFLATOR WAS NOT INCLUDED IN THE RECTAL CATHETER. WHAT GOOD IS THE ITEM IF THEY COULD NOT INFLATE OR DEFLATE THE BALLOON. THEY USED TO SELL THIS ITEM YEARS AGO WITH THE BULB INFLATOR. PERHAPS THEY COULD TELL HOW TO INFLATE AND DEFLATE THE BALLOON ON THIS RECTAL CATHETER. THEY WOULD PURCHASE IF IT HAD THE BULB INFLATOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18208940 ↗MalfunctionMay 11, 2017Failure to Infuse
IT WAS REPORTED THAT THE DEVICE WOULD NOT INFUSE DURING PRETESTING.
Patient problems: No Patient Involvement
MAUDE report 6562171 ↗
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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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