Medline MSC091080Recalls & reported problems
Medline Industries, Inc. · LIQUIBAND SECURE WOUND CLOSURE, 66CM · Class 2
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 10197344009404), received between Sep 17, 2026 and Sep 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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
- Loss of or Failure to Bond1
- No Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Wound Dehiscence1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026No Flow
It was reported that "THE LIQUID WILL NOT DROP FULLY TO THE FOAM END."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50871209 ↗MalfunctionSep 17, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions; Wound Dehiscence
MAUDE report 50811401 ↗
Other Cutaneous tissue adhesive with mesh devices
- DERMABOND PRINEO CLR222USEthicon, LLC · Cutaneous tissue adhesive with mesh790 reports
- DERMABOND PRINEO CLR222Ethicon, LLC · Cutaneous tissue adhesive with mesh183 reports
- DERMABOND PRINEO CLR602USEthicon, LLC · Cutaneous tissue adhesive with mesh80 reports
- DERMABOND PRINEO CLR422USEthicon, LLC · Cutaneous tissue adhesive with mesh46 reports
- Exofin Fusion Skin Closure System 22cmChemence Medical, Inc. · Cutaneous Tissue Adhesive With Mesh1 report
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