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
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
- CVS Health 894111Woonsocket Prescription Center, Incorporated · Gauze / Sponge,Nonresorbable For External Use1 recall0 reports
- MEDLINE INDUSTRIES, INC. NON25212Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use5 reports
- MEDLINE INDUSTRIES, INC. PRM21408CMedline Industries, Inc. · Gauze / sponge,nonresorbable for external use4 reports
- Curad CUR47397RBMedline Industries, Inc. · Gauze / sponge,nonresorbable for external use4 reports
- CURAD NON25700Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use3 reports
- Medline NON25865Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use2 reports
- MEDLINE NON25441Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use2 reports
- CURAD NON25710Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use2 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page