Curad CURCC300Recalls & reported problems
Medline Industries, Inc. · DBD-CURAD,BANDAGES,ASST,300CT/BX-CASE · Class 1
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 00888277420031), received between Sep 10, 2026 and Sep 16, 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
- Adhesive Too Strong2
- Patient Device Interaction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Skin Tears3
- Erythema2
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794060 ↗MalfunctionSep 16, 2026Loss of or Failure to Bond
It was reported that "when I received them and went to use one, it didn't stick. This happened with four more band-aids, all not sticking until I eventually gave up and went without a band-aid."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50786407 ↗MalfunctionSep 15, 2026Patient Device Interaction Problem
It was reported that "I used a bandaid of yours the other day and when taking it off it actully tore a piece of skin off with it."
Patient problems: Skin Tears
MAUDE report 50771662 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
It was reported that "THE ENTIRE BOX OF BANDAGES ARE JUST FALLING OFF WITHIN MINUTES" and "IT FEELS AS IF THERE IS BARELY ANY ADHESIVE ON THEM."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50753250 ↗MalfunctionSep 13, 2026Adhesive Too Strong
Patient problems: Erythema; Skin Tears
MAUDE report 50747485 ↗MalfunctionSep 12, 2026Adhesive Too Strong
Patient problems: Erythema; Hemorrhage/Blood Loss/Bleeding; Skin Tears
MAUDE report 50746553 ↗MalfunctionSep 10, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50721708 ↗
Other Tape and bandage, adhesive devices
- IV3000-1-HAND 10X12CM-CARTON OF 50 66024008Smith & Nephew Medical Limited · Tape And Bandage, Adhesive62 reports
- CURAD NON25600QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall2 reports
- IV3000-1-HAND 6X7CM-CARTON OF 100 66024007Smith & Nephew Medical Limited · Tape And Bandage, Adhesive52 reports
- 3M™ 1500U3m Company · Tape and bandage, adhesive1 recall1 report
- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
- CURAD NON256133QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall0 reports
- CURAD NON25660QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall0 reports
- Seer Home SM-01-9005Seer Medical Holdings Limited · Tape And Bandage, Adhesive1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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