Skip to content

Dover 605163ICRecalls & reported problems

Cardinal Health, Inc. · Silver Coated 100% Silicone Foley Catheter,5 mL, 2-Way · Class 2

All models of Dover (90)

Data updated Oct 16, 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 10884521026452), received between Mar 31, 2021 and Mar 31, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

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.

  • MalfunctionMar 31, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    THE CUSTOMER REPORTED THAT THE CATHETER BROKE APART WHERE THE TWO-WAY PRONG CONNECTS TO THE TUBE. THERE WAS NO PATIENT INJURY, THE ISSUE OCCURRED BEFORE THE NURSE INSERTED THE CATHETER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11599875 ↗

Other CATHETER, RETENTION TYPE, BALLOON devices

All CATHETER, RETENTION TYPE, BALLOON devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page