Medline MSC091050Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10888277728608), received between Dec 19, 2023 and Sep 16, 2026 — classified as 3 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 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 50786113 ↗
• MalfunctionSep 8, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50675950 ↗
• MalfunctionApr 3, 2026Material Fragmentation; Material Separation

  ACCORDING TO THE FACILITY, A PHYSICIAN ATTEMPTED TO APPLY OPTICLOSE TO A WOUND USING THE NEW SKIN GLUE APPLICATOR IN A NORMAL MANNER. UPON BREAKING THE AMPULE USING THE WINGS, THE TOP DISLODGED AND THE INTERNAL GLASS AMPULE SHATTERED, RESULTING IN GLASS SHARDS CONTACTING THE PATIENT'S SKIN AND INCISION SITE. THE SITE WAS CLEANED AND RE SOAKED WITH IRRISEPT, AND STERI STRIPS WERE USED TO COMPLETE THE CASE. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.

  Patient problems: Foreign Body In Patient

  MAUDE report 24776752 ↗
• InjuryApr 22, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER, "PHYSICIANS ARE COMPLAINING THEY HAVE TRIED THE LIQUIBAND IT DOES NOT ADHERE WELL TO THE WOUND, WE HAVE PATIENTS COMING BACK BECAUSE THEIR WOUNDS ARE OPENING UP".

  Patient problems: Insufficient Information

  MAUDE report 19153810 ↗
• InjuryMar 18, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER, THE ADHESIVE WAS USED ON AN INCISION AFTER AN "EXCISION FOR SQUAMOUS CELL CANCER OF SKIN" ON THE "LEFT CHEEK" ON (B)(6) 2024 AND "LATER THAT EVENING" THE PATIENT HAD "BLEEDING".

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 18922252 ↗
• InjuryDec 19, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON (B)(6) 2023 "THE TIP OF THE APPLICATED FELL OFF WHEN THE PRODUCT WAS SQUEEZED FOR APPLICATION".

  Patient problems: Foreign Body In Patient

  MAUDE report 18355396 ↗