CURAD CURIM1850V1Recalls & reported problems
Medline Industries, Inc. · IRONMAN, BNDG,ANTIBAC,VARIETY PACK,50CT · Class U
All models of CURAD (85)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00193489023421), received between Aug 13, 2026 and Sep 21, 2026 — classified as 1 injury, 7 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (3 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 Bond3
- Adhesive Too Strong2
- Biocompatibility2
- Patient Device Interaction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Pain3
- Skin Tears3
- Blister1
- Caustic/Chemical Burns1
- Discomfort1
- Skin Discoloration1
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Biocompatibility
Patient problems: Discomfort; Pain; Skin Tears
MAUDE report 50840533 ↗MalfunctionSep 16, 2026Patient Device Interaction Problem
Patient problems: Skin Inflammation/ Irritation; Skin Tears
MAUDE report 50794296 ↗MalfunctionSep 15, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50775703 ↗MalfunctionSep 15, 2026Adhesive Too Strong
Patient problems: Pain; Skin Tears
MAUDE report 50773870 ↗MalfunctionSep 14, 2026Adhesive Too Strong
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50763124 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50762651 ↗MalfunctionSep 11, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50740373 ↗InjuryAug 13, 2026Biocompatibility
It was reported that "My son had a red splotchy spot on his arm so I placed a curad bandage on the area before he went to daycare."
Patient problems: Blister; Caustic/Chemical Burns; Pain; Skin Discoloration
MAUDE report 50242722 ↗
Other Dressing, wound, drug devices
- MediHoney® 31815Acell, Inc. · Dressing, wound, drug2 recalls7 reports
- MediHoney® 31515Acell, Inc. · Dressing, wound, drug2 recalls6 reports
- MediHoney® 31805Acell, Inc. · Dressing, wound, drug2 recalls1 death5 reports
- MediHoney® 31535Acell, Inc. · Dressing, wound, drug2 recalls0 reports
- AQUACEL AG FOAM 420681Convatec, Purchasing Department · Dressing, Wound, Drug99 reports
- SteriCare Solutions 6240Nurse Assist, Inc. · Dressing, Wound, Drug1 recall14 reports
- Medline DYND500MLSMedline Industries, Inc. · Dressing, wound, drug1 recall5 reports
- MEDLINE MNK0005Medline Industries, Inc. · Dressing, wound, drug1 recall5 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