Skip to content

CURAD NON25670Recalls & reported problems

Medline Industries, Inc. · BANDAGE, ADHESIVE, WTRPRF, 1"X3", ST, LF · Class 1

Adverse event reports
14
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 00888277367183), received between Sep 10, 2026 and Sep 30, 2026 — classified as 13 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

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: 14 reportsOct 2026: 0 reports20242025202614
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Loss of or Failure to Bond8
  • Product Quality Problem4
  • Adhesive Too Strong1
  • Difficult to Open or Remove Packaging Material1
  • Inadequacy of Device Shape and/or Size1

Patient problems

  • No Clinical Signs, Symptoms or Conditions13
  • Skin Inflammation/ Irritation1
  • Unspecified Infection1

Recent adverse event reports

The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50951923 ↗
  • MalfunctionSep 30, 2026Loss of or Failure to Bond

    It was reported that the band aids are not waterproof as they say on the box.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50949365 ↗
  • MalfunctionSep 29, 2026Product Quality Problem; Difficult to Open or Remove Packaging Material

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50934139 ↗
  • MalfunctionSep 22, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50861344 ↗
  • MalfunctionSep 16, 2026Product Quality Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50788459 ↗
  • MalfunctionSep 15, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50779454 ↗
  • MalfunctionSep 13, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50747784 ↗
  • MalfunctionSep 13, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50747642 ↗
  • MalfunctionSep 12, 2026Product Quality Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50746306 ↗
  • MalfunctionSep 11, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50743526 ↗
  • MalfunctionSep 11, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50735470 ↗
  • MalfunctionSep 11, 2026Adhesive Too Strong

    It was reported that the adhesive was really strong that he felt his skin was going to peel when he was trying to remove the bandage.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50732702 ↗
  • MalfunctionSep 10, 2026Inadequacy of Device Shape and/or Size

    Patient problems: Skin Inflammation/ Irritation; Unspecified Infection

    MAUDE report 50717888 ↗
  • OtherSep 10, 2026Product Quality Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50716911 ↗

Other Tape and bandage, adhesive devices

All Tape and bandage, adhesive devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.