CURAD NON25710Recalls & reported problems
Medline Industries, Inc. · PAD,NON-ADHERENT,3X4,STERILE,LF,1/PK · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196740147), received between Sep 11, 2026 and Sep 22, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
- Material Discolored1
- Patient-Device Incompatibility1
- Physical Resistance/Sticking1
Patient problems
- Hypersensitivity/Allergic reaction1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Improper or Incorrect Procedure or Method; Patient-Device Incompatibility; Physical Resistance/Sticking
Patient problems: Hypersensitivity/Allergic reaction
MAUDE report 50860522 ↗MalfunctionSep 11, 2026Material Discolored
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50736594 ↗
Other Gauze / sponge,nonresorbable for external use devices
- CVS Health 894111Woonsocket Prescription Center, Incorporated · Gauze / Sponge,Nonresorbable For External Use1 recall0 reports
- Curad CUR47147RBMedline Industries, Inc. · Gauze / sponge,nonresorbable for external use9 reports
- MEDLINE INDUSTRIES, INC. NON25212Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use5 reports
- Curad CUR47397RBMedline Industries, Inc. · Gauze / sponge,nonresorbable for external use4 reports
- MEDLINE INDUSTRIES, INC. PRM21408CMedline Industries, Inc. · Gauze / sponge,nonresorbable for external use4 reports
- CURAD NON25700Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use3 reports
- MEDLINE NON25441Medline Industries, Inc. · Gauze / sponge,nonresorbable for external use2 reports
- MEROCEL® 470404Medtronic Xomed, Inc. · Gauze / sponge,nonresorbable for external use2 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.
How reports and recalls are matched · Editorial policy · Report an error on this page