CURAD NON25660Recalls & reported problems
Medline Industries, Inc. · BANDAGE,ADHESIVE,FABRIC,1"X3",STRL,LF · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00080196692791), received between Sep 12, 2026 and Sep 30, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (6 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond6
- Adhesive Too Strong2
- Interrogation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
- Skin Tears2
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952532 ↗MalfunctionSep 24, 2026Loss of or Failure to Bond
It was reported that "BANDAGE NOT STICKING ON SKIN."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50882383 ↗MalfunctionSep 21, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50845935 ↗MalfunctionSep 15, 2026Loss of or Failure to Bond
It was reported that NONE OF THE BANDAGES ARE STICKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50772767 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
It was reported that "She said that they are not as sticky as they used to be" and she said they fall off more frequently than in the past."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50752335 ↗MalfunctionSep 13, 2026Interrogation Problem
Patient problems: Hemorrhage/Blood Loss/Bleeding; Skin Tears
MAUDE report 50747619 ↗MalfunctionSep 13, 2026Adhesive Too Strong
Patient problems: Skin Tears
MAUDE report 50747043 ↗MalfunctionSep 13, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50747012 ↗MalfunctionSep 12, 2026Adhesive Too Strong
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746676 ↗
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
- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
- 3M™ 1500U3m Company · Tape and bandage, adhesive1 recall1 report
- NG Strip™ NG-25Derma Sciences Canada Inc · Tape and bandage, adhesive1 recall0 reports
- Lucky Super Soft Bandages in differenet sizeDelta Brands 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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