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Curad CUR47147RBRecalls & reported problems

Medline Industries, Inc. · PAD,NON-STICK,CURAD,W/ADH,2X3,ST,20/BX · Class 1

All models of CURAD (85)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
9
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00080196300023), received between Sep 9, 2026 and Sep 29, 2026 — classified as 9 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (6 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 9 reportsOct 2026: 0 reports2024202520269
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Loss of or Failure to Bond6
  • Adhesive Too Strong1
  • Component Missing1
  • Material Split, Cut or Torn1
  • Physical Resistance/Sticking1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6
  • Unspecified Tissue Injury2
  • Pain1

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 29, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50932180 ↗
  • MalfunctionSep 16, 2026Component Missing

    Patient problems: Unspecified Tissue Injury

    MAUDE report 50794190 ↗
  • MalfunctionSep 16, 2026Physical Resistance/Sticking

    It was reported that "SHE HAD THE PAD ON HER WOUND FOR ABOUT 4 HOURS. WHEN SHE WENT TO REMOVE IT, IT STUCK TO HER WOUND SO MUCH SHE COULDNT GET IT OFF WITHOUT IT HURTING HER WOUND."

    Patient problems: Pain

    MAUDE report 50793809 ↗
  • MalfunctionSep 15, 2026Loss of or Failure to Bond; Material Split, Cut or Torn

    It was reported that "PADS ARE FALLING APART AND ADHESIVE TABS DON'T STICK".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50778500 ↗
  • MalfunctionSep 12, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50746261 ↗
  • MalfunctionSep 11, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50734030 ↗
  • MalfunctionSep 10, 2026Loss of or Failure to Bond

    It was reported that "THE LAYERS OF THICKNESS SEEM TOO LOOSE AS WELL AS THE ADHESIVE ITSELF" and "SHE HAD TO USE MEDICAL TAPE TO KEEP THE ITEM FROM FALLING OFF HER LEG DUE TO THE ADHESIVE NOT BEING STICKY ENOUGH."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50721596 ↗
  • MalfunctionSep 10, 2026Adhesive Too Strong

    Patient problems: Unspecified Tissue Injury

    MAUDE report 50715629 ↗
  • MalfunctionSep 9, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50700038 ↗

Other Gauze / sponge,nonresorbable for external use devices

All Gauze / sponge,nonresorbable for external use devices →

Sources and updates

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