CURAD CURIM5018V1Recalls & reported problems
Medline Industries, Inc. · BNDG,ANTIBAC,IRONMAN,XL,6-COLORS,10CT · Class U
All models of CURAD (85)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00193489023445), received between Sep 11, 2026 and Sep 17, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Adhesive Too Strong” (1 report).
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
- Adhesive Too Strong1
- Appropriate Device Problem Term/Code Not Available1
- Biocompatibility1
Patient problems
- Erythema1
- Hemorrhage/Blood Loss/Bleeding1
- No Clinical Signs, Symptoms or Conditions1
- Skin Tears1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 17, 2026Appropriate Device Problem Term/Code Not Available
Patient problems: Erythema; Hemorrhage/Blood Loss/Bleeding
MAUDE report 50811612 ↗MalfunctionSep 15, 2026Adhesive Too Strong
Patient problems: Skin Tears
MAUDE report 50780579 ↗MalfunctionSep 11, 2026Biocompatibility
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50742715 ↗
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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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