CURAD CUR1625V1Recalls & reported problems
Medline Industries, Inc. · KIT,WOUNDCARE,ASSORTED,25CT · Class 1
All models of CURAD (85)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00884389101868), received between Sep 9, 2026 and Sep 18, 2026 — classified as 4 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond4
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Unspecified Tissue Injury1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 18, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829141 ↗MalfunctionSep 12, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746457 ↗MalfunctionSep 10, 2026Loss of or Failure to Bond
Patient problems: Unspecified Tissue Injury
MAUDE report 50719185 ↗MalfunctionSep 9, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50695774 ↗
Other First aid kit without drug devices
- NAR Kit 85-0740North American Rescue, LLC · First Aid Kit Without Drug1 recall0 reports
- Ptensys Bleeding Control Station TM-400TyTek Medical Inc. · First Aid Kit Without Drug1 recall0 reports
- CVS Health 998842Woonsocket Prescription Center, Incorporated · First Aid Kit Without Drug1 recall0 reports
- Lucky Super Soft KitDelta Brands Inc. · First Aid Kit Without Drug1 recall0 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