CURE CATHETER CLOSED SYSTEM CS14CRecalls & reported problems
Convatec, Purchasing Department · Catheter Closed System Kit, Coude Tip · Class 2
All models of CURE CATHETER CLOSED SYSTEM (4)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815947020697), received between Nov 6, 2020 and Nov 6, 2020 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Urinary Tract Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 6, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
INTERMITTENT CATHETER PATIENT (USER) STATED HE IS CURRENTLY BEING TREATED BY HIS DOCTOR FOR A URINARY TRACT INFECTION (UTI) CONCURRENT WITH CATHETER USE. DURING FOLLOW-UP, THE PATIENT SAID HE HAS TAKEN FIVE DIFFERENT COURSES OF DIFFERENT ANTIBIOTICS AND IS STILL INFECTED. HE WAS THEN PLACED ON A SEVEN DAY COURSE OF SHOTS WHICH REQUIRE HIM TO GO TO THE HOSPITAL EACH DAY TO RECEIVE WITH HOPE THAT THE TREATMENT WILL CAUSE HIM TO RECOVER FROM THE INFECTION.
Patient problems: Urinary Tract Infection
MAUDE report 10803651 ↗
Other Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) devices
- Bard® Touchless® Plus Unisex Pre-Lubricated Vinyl Urethral Catheter Kit 4A5144C. R. Bard, Inc. · Tray, catheterization, sterile urethral, with or without catheter (kit)170 reports
- Bard® Touchless® Plus Unisex Pre-Lubricated Rubber Urethral Catheter Kit 4A7044C. R. Bard, Inc. · Tray, catheterization, sterile urethral, with or without catheter (kit)54 reports
- Dover 3450LFCardinal Health, Inc. · Tray, catheterization, sterile urethral, with or without catheter (kit)1 recall3 reports
- Dover 3450Cardinal Health, Inc. · Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)1 recall1 report
- Dover 8887600776Cardinal Health, Inc. · Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)1 recall0 reports
- Dover 3420Cardinal Health, Inc. · Tray, catheterization, sterile urethral, with or without catheter (kit)1 recall0 reports
- Dover 3410Cardinal Health, Inc. · Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)1 recall0 reports
- Dover 2480Cardinal Health, Inc. · Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)1 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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