Skip to content

Medline UROT1061Recalls & reported problems

Medline Industries, Inc. · DBD-TRAY TTL VENT 100%SILI UM 18FR · Class 2

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 10193489513059), received between Feb 27, 2020 and Feb 27, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Remove” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Difficult to Remove1

Patient problems

  • No Code Available1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 27, 2020Difficult to Remove

    IT WAS REPORTED THAT THE URINARY CATHETER WAS DIFFICULT TO REMOVE.

    Patient problems: No Code Available

    MAUDE report 9763424 ↗

Other Catheter care tray devices

All Catheter care tray devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.