LiquiBand Exceed LX6Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10884521543430), received between Apr 14, 2022 and Oct 15, 2025 — classified as 4 injuries, 3 malfunctions.

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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT DURING THE CLOSING (SKIN) STEP OF A LAPAROSCOPIC APPENDECTOMY, THE USE OF SKIN ADHESION WAS ASSOCIATED WITH A TISSUE REACTION CHARACTERIZED BY SKIN IRRITATION, POSTOPERATIVE SKIN REACTION, AND DELAYED CONTACT ALLERGY TO THE SURGICAL GLUE. RAISED ERYTHEMATOUS VESICLES AND PUSTULES WERE OBSERVED SURROUNDING AREAS OF SURGICAL GLUE AND DISSEMINATING AROUND THESE AREAS ON THE LEFT ABDOMEN. ADDITIONAL SYMPTOMS INCLUDED REDNESS, ITCHINESS, AND BUMPS AT THE INCISIONAL SITES. THE PATIENT, WHO HAD A MEDICAL HISTORY OF ECZEMA AND MIGRAINES, REPORTED FEELING GENERALLY WELL SINCE SURGERY EXCEPT FOR CONCERN ABOUT THE REDNESS AND ITCHINESS AT THE INCISIONAL SITES, WHICH WERE FIRST NOTICED TWO WEEKS AFTER SURGERY. THE PATIENT DENIED FEVER, AND NO OBVIOUS SIGNS OF INFECTION, INCREASED WARMTH, OR TENDERNESS WERE NOTED ON PHYSICAL EXAMINATION BY HEALTHCARE PROFESSIONALS AT THE POSTOPERATIVE VISIT. TREATMENT INCLUDED TOPICAL HYDROCORTISONE AND BENADRYL CREAMS, ORAL BENADRYL AND GENERIC CLARITIN AS NEEDED, ICE APPLICATION, AND BANDAGING FOR IRRITATION FROM CLOTHING PROTECTION.

  Patient problems: Abscess; Hypersensitivity/Allergic reaction

  MAUDE report 23302524 ↗
• MalfunctionJun 19, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, POSTOPERATIVELY, AFTER AN OPEN BREAST PROCEDURE, THE PATIENT RETURNED TWO MONTHS AGO WITH SKIN REACTIONS. THE REACTIONS FOLLOWED THE BROAD DISTRIBUTION OF THE SKIN PREP CALLED CHLOROPREP. SKIN PREP WAS CHANGED TO BETADINE A MONTH AGO, AND THE PATIENT HAS NOT HAD ANY SKIN REACTIONS SINCE. THE DOCTOR COULD NOT RULE OUT TRANSCORTICAL SENSORY APHASIA (TSA) AS THE CAUSE YET BUT THINKS IT WAS LIKELY DUE TO THE SKIN PREPARATION. THE DOCTOR WAS ALSO AWARE THAT A SMALL PERCENT OF PATIENTS HAD REACTIONS TO CYANOACRYLATES AND HAD SEEN PATIENTS WITH MORE CENTRAL REACTIONS THAT WERE PROBABLY TSA WITH THE SKIN ADHESIVE.

  Patient problems: Hypersensitivity/Allergic reaction

  MAUDE report 19571062 ↗
• MalfunctionJun 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ACCORDING TO THE REPORTER, FOLLOWING AN OPEN BREAST PROCEDURE, THE PATIENT HAD SKIN REACTIONS. THE REACTIONS FOLLOWED THE BROAD DISTRIBUTION OF THE SKIN PREP CALLED CHLORO PREP. SKIN PREP WAS THEN CHANGED TO BETADINE A MONTH AGO AND THE PATIENT DID NOT HAVE ANY SKIN REACTIONS SINCE.

  Patient problems: Hypersensitivity/Allergic reaction

  MAUDE report 19558336 ↗
• InjuryApr 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  OCCURRENCE OF REDNESS 2 TO 3 WEEKS AFTER THE GLUE APPLICATION, AFTER MAMMARY SURGERY. NO FURTHER DETAILS AT THIS TIME.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 14112943 ↗
• InjuryApr 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  OCCURRENCE OF REDNESS 2 TO 3 WEEKS AFTER THE GLUE APPLICATION, AFTER MAMMARY SURGERY. NO FURTHER DETAILS AT THIS TIME.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 14112874 ↗
• InjuryApr 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  OCCURRENCE OF REDNESS 2 TO 3 WEEKS AFTER THE GLUE APPLICATION, AFTER MAMMARY SURGERY. NO FURTHER DETAILS AT THIS TIME.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 14112779 ↗
• InjuryApr 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  OCCURRENCE OF REDNESS 2 TO 3 WEEK AFTER THE GLUE APPLICATION, AFTER MAMMARY SURGERY. NO FURTHER DETAILS AT THIS TIME.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 14111434 ↗