Curad CUR47315RRBRecalls & reported problems
Medline Industries, Inc. · BANDAGE,FABRIC,CURAD,30CT,3/4X3" · Class 1
All models of CURAD (85)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 00080196300214), received between May 29, 2026 and Sep 29, 2026 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (8 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 Bond8
- Degraded2
- Adhesive Too Strong1
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
- Insufficient Information1
- Skin Tears1
- Unspecified Tissue Injury1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Degraded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936664 ↗MalfunctionSep 15, 2026Loss of or Failure to Bond
Patient problems: Unspecified Tissue Injury
MAUDE report 50778890 ↗MalfunctionSep 14, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50763310 ↗MalfunctionSep 13, 2026Degraded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746974 ↗MalfunctionSep 12, 2026Adhesive Too Strong
Patient problems: Skin Tears
MAUDE report 50746510 ↗MalfunctionSep 12, 2026Product Quality Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746154 ↗MalfunctionSep 11, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744540 ↗MalfunctionSep 11, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50740385 ↗MalfunctionSep 10, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50717504 ↗MalfunctionSep 9, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50695523 ↗MalfunctionSep 8, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676765 ↗MalfunctionMay 29, 2026Loss of or Failure to Bond
IT WAS REPORTED THAT BANDAGES DO NOT STICK.
Patient problems: Insufficient Information
MAUDE report 25340664 ↗
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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