Curad NON75100Recalls & reported problems
Medline Industries, Inc. · SILICONE FABRIC ADH BNDG 3/4X3 · Class 1
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 20888277677750), received between Aug 27, 2026 and Sep 22, 2026 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (8 reports).
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
- Loss of or Failure to Bond8
- Adhesive Too Strong1
- Component Misassembled1
- Component Missing1
- Device Contaminated During Manufacture or Shipping1
- Device Slipped1
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions11
- Pain1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Adhesive Too Strong
It was reported that "the bandages in the last box I brought stuck to my skin like they were regular bandages and definitely were not Ouchless.."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50853740 ↗MalfunctionSep 15, 2026Loss of or Failure to Bond
It was reported that the silicone fabric does not stick.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778640 ↗MalfunctionSep 15, 2026Device Slipped
Patient problems: Pain
MAUDE report 50777645 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765022 ↗MalfunctionSep 14, 2026Product Quality Problem; Component Missing; Component Misassembled
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50763586 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
It was reported that "This specific box (LOT 10321100001) has adhesive that is not working properly. It does not stick fully when first applied and falls off." It was also reported that "the cloth material on the inside is different than how it should look. The ones from this box have smaller square pieces with less coverage."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50758427 ↗MalfunctionSep 14, 2026Device Contaminated During Manufacture or Shipping
It was reported that "I just opened one and the non-stick pad is black?"
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50754390 ↗MalfunctionSep 12, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746808 ↗MalfunctionSep 12, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50745176 ↗MalfunctionSep 9, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698200 ↗MalfunctionSep 8, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675108 ↗MalfunctionAug 27, 2026Loss of or Failure to Bond
It was reported that the bandages do not stick. The ends keep coming off and happens before 30 min.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50485626 ↗
Other Dressing, wound, hydrophilic devices
- MEDLINE INDUSTRIES, INC. MSC7044EPMedline Industries, Inc. · Dressing, wound, hydrophilic1 recall1 report
- McKesson 3561Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic1 recall0 reports
- McKesson 3562Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic1 recall0 reports
- McKesson 3563Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic1 recall0 reports
- McKesson 87400Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic1 recall0 reports
- DuPad® 87810Derma Sciences Canada Inc · Dressing, wound, hydrophilic1 recall0 reports
- McKesson 3564Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic1 recall0 reports
- MAXORB EXTRA AlginateMedline Industries, Inc. · Dressing, Wound, Hydrophilic1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.