Bard® Goodwin Sound 042822Recalls & reported problems
C. R. Bard, Inc. · Bard Goodwin Sound Open Tip 22 Fr. · Class 1
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 00801741047275), received between Jul 7, 2020 and Jul 7, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Corroded” (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.
Most reported problems
Device problems
- Corroded1
Patient problems
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 7, 2020Corroded
IT WAS REPORTED THAT THE GOODWIN SOUND DILATORS HAD DETERMINED TO BE RUSTING INSIDE THE LUMEN OF THE SOUND. PER FOLLOW UP INFORMATION RECEIVED VIA EMAIL ON 24JUN2020, THE COMPLAINANT PROVIDED SIX PRODUCT CATALOG NUMBER WITH THE ISSUE.
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 10240711 ↗
Other SOUND, URETHRAL, METAL OR PLASTIC devices
- Bard® Goodwin Sound 042812C. R. Bard, Inc. · SOUND, URETHRAL, METAL OR PLASTIC4 reports
- Bard® Goodwin Sound 042830C. R. Bard, Inc. · SOUND, URETHRAL, METAL OR PLASTIC3 reports
- Bard® Goodwin Sound 042828C. R. Bard, Inc. · SOUND, URETHRAL, METAL OR PLASTIC2 reports
- Bard® Goodwin Sound 042824C. R. Bard, Inc. · SOUND, URETHRAL, METAL OR PLASTIC2 reports
- Bard® Goodwin Sound 042820C. R. Bard, Inc. · SOUND, URETHRAL, METAL OR PLASTIC2 reports
- Bard® Goodwin Sound 042826C. R. Bard, Inc. · SOUND, URETHRAL, METAL OR PLASTIC2 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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