MEDLINE MSC3266Recalls & reported problems
Medline Industries, Inc. · GAUZE,BORDER,6"X6",4"X4"PAD,STERILE · Class 1
- 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 10080196743063), received between Sep 15, 2026 and Sep 23, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Biocompatibility” (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.
Reports received per month
Most reported problems
Device problems
- Biocompatibility1
- Difficult to Open or Close1
- Loss of or Failure to Bond1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Contact Dermatitis1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Loss of or Failure to Bond
It was reported that "These bandages are not sticky."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870256 ↗MalfunctionSep 22, 2026Difficult to Open or Close
It was reported that THEY ARE NOT ABLE TO OPEN THE GAUZE FROM THE PAPER LINER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854415 ↗MalfunctionSep 15, 2026Biocompatibility
Patient problems: Contact Dermatitis
MAUDE report 50779056 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.