MEDLINE INDUSTRIES, INC. MSC3236Recalls & reported problems
Medline Industries, Inc. · GAUZE, BORDER, 3"X6", 1.5"X4"PAD, STERIL · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30888277678976), received between Sep 9, 2026 and Sep 22, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Degraded” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Degraded1
- Loss of or Failure to Bond1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Skin Inflammation/ Irritation1
- Tissue Breakdown1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Loss of or Failure to Bond; Degraded
It was reported that "THE ADHESIVE MELTED AND IT BECAME GUMMY AND DOESNT STICK TO HIS SKIN."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854887 ↗MalfunctionSep 16, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50791835 ↗MalfunctionSep 9, 2026Adverse Event Without Identified Device or Use Problem
It was reported that ¿per caller- skin reaction to the dressing (been using for 5 days) very irritated, getting a rash and skin break down.¿
Patient problems: Skin Inflammation/ Irritation; Tissue Breakdown
MAUDE report 50694078 ↗
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- DUODERM 187662Convatec, Purchasing Department · Dressing, Wound, Occlusive43 reports
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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