Bard® Universal Catheterization Tray 792100Recalls & reported problems
C. R. Bard, Inc. · Bard® Universal Catheterization Tray · Class 2
Data updated Oct 16, 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 00801741029646), received between Feb 15, 2019 and Jul 2, 2019 — 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 16, 2026.
Most reported problems
Device problems
- Component Missing1
- Inadequate Instructions for Healthcare Professional1
- Packaging Problem1
Patient problems
- No Known Impact Or Consequence To Patient2
- No Patient Involvement2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 2, 2019Component Missing
IT WAS REPORTED THAT THE TRAY DID NOT CONTAIN THE IODINE SWABSTICKS.
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 8754356 ↗MalfunctionFeb 15, 2019Inadequate Instructions for Healthcare Professional; Packaging Problem; Inadequate Instructions for Healthcare Professional
IT WAS REPORTED THAT THE CATHETER TRAY (792100) WAS IN A CASE OF INTERMITTENT CATHETER TRAYS (770715).
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 8342688 ↗
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- Centurion Medical Products Corp CVI680CMedline Industries, Inc. · Catheter care tray2 recalls0 reports
- Bardia® Foley Catheter Insertion Tray 802010C. R. Bard, Inc. · Catheter care tray54 reports
- Medline DYND10160Medline Industries, Inc. · Catheter care tray1 recall4 reports
- Medline DYNC1816Medline Industries, Inc. · Catheter care tray1 recall2 reports
- SureStep Intermittent Catheter Tray INTAAIC. R. Bard, Inc. · Catheter care tray1 recall1 report
- Medline DYND10407Medline Industries, Inc. · Catheter care tray1 recall1 report
- Centurion Medical Products Corp IVS3635BMedline Industries, Inc. · Catheter care tray1 recall0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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