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Medline Industries, Inc. DYNDC2395ARecalls & reported problems

Medline Industries, Inc. · DRESSING CHANGE TRAY · Class 2

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 10889942781843), received between Sep 4, 2019 and Sep 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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

  • Contamination /Decontamination Problem1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionSep 4, 2019Contamination /Decontamination Problem

    IT WAS REPORTED THAT "FUZZ PARTICLES" WERE COMING OFF THE SWAB STICK (TAKEN FROM DRESSING CHANGE TRAY). PER REPORT, THE FUZZ PARTICLES HAD IMBEDDED DOWN INTO THE SKIN AND WERE NOT ABLE TO BE REMOVED.

    Patient problems: No Information

    MAUDE report 8960014 ↗

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Sources and updates

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