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MEDLINE INDUSTRIES, INC. NON7915Recalls & reported problems

Medline Industries, Inc. · DRESSING,BURN,18"X18",50PLY,STERILE,LF · Class 1

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 10080196288656), received between Apr 8, 2021 and Apr 8, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Product Quality 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

  • Product Quality Problem1

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.

  • MalfunctionApr 8, 2021Product Quality Problem

    IT HAS BEEN REPORTED, STERILE BURN DRESSINGS, 18" X 18 "IS SHEDDING QUITE A BIT AND EMBEDDING INTO WOUNDS AND THEY THEN HAVE TO PICK PIECES OUT."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11634630 ↗

Other Gauze / sponge,nonresorbable for external use devices

All Gauze / sponge,nonresorbable for external use devices →

Sources and updates

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