CURAD CURIM5021V1Recalls & reported problems
Medline Industries, Inc. · BNDG,ANTIBAC,IRONMAN,FNG/KNK,6-CLR,20CT · Class U
All models of CURAD (85)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00193489023476), received between Sep 12, 2026 and Sep 29, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (4 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond4
- Biocompatibility2
- Improper or Incorrect Procedure or Method2
- Adhesive Too Strong1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
- Scar Tissue2
- Skin Inflammation/ Irritation2
- Skin Tears2
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Improper or Incorrect Procedure or Method; Biocompatibility
Patient problems: Scar Tissue; Skin Inflammation/ Irritation; Skin Tears
MAUDE report 50931988 ↗MalfunctionSep 23, 2026Loss of or Failure to Bond
It was reported that "they do not stay stuck. I have a photo of where it's coming unstuck from my knuckle in an area."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872685 ↗MalfunctionSep 21, 2026Improper or Incorrect Procedure or Method; Biocompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions; Scar Tissue; Skin Inflammation/ Irritation; Skin Tears
MAUDE report 50847089 ↗MalfunctionSep 15, 2026Loss of or Failure to Bond
It was reported that the bandages do not stick.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777925 ↗MalfunctionSep 15, 2026Adhesive Too Strong
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773686 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
It was reported that "It appears that both sets of these have very little if any adhesive hold to them. I used numerous bandages from both boxes, often having to replace the bandage within 15 to 30 minutes."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756395 ↗MalfunctionSep 12, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746281 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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