LIGACLIP LX110Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 20705036012860), received between May 1, 2019 and Aug 15, 2024 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Failure to Form Staple” (6 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 16, 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.

• MalfunctionAug 15, 2024Failure to Form Staple; Failure to Form Staple

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE CLIPS WERE SCISSORING WHEN THEY WERE BEING DEPLOYED. CASE WAS COMPLETED WITHOUT PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19992944 ↗
• MalfunctionApr 11, 2024Unintended Ejection; Failure to Form Staple; Unintended Ejection; Failure to Form Staple

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE CLIPS ARE NOT CLIPPING PROPERLY AND ARE NOT EFFECTIVE. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19091846 ↗
• MalfunctionMar 5, 2024Unintended Ejection; Failure to Form Staple; Insufficient Device Problem Information; Unintended Ejection; Failure to Form Staple; Insufficient Device Problem Information

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE CLIPS AREN'T CLIPPING PROPERLY AND AREN'T EFFECTIVE. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18840355 ↗
• MalfunctionMar 5, 2024Unintended Ejection; Failure to Form Staple; Unintended Ejection; Failure to Form Staple

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE CLIPS AREN'T CLIPPING PROPERLY AND AREN'T EFFECTIVE. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18839514 ↗
• MalfunctionDec 15, 2023Failure to Form Staple; Failure to Form Staple

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, WHEN CLOSING THE CLIPS, THEY WEREN'T CLOSING IN THE PATTERN/FORM THEY WERE SUPPOSED TO. SOME ALSO APPEARED TO BE A BIT CROOKED AS WELL. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18335421 ↗
• MalfunctionDec 15, 2023Failure to Form Staple; Failure to Form Staple

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, WHEN CLOSING THE CLIPS, THEY WEREN'T CLOSING IN THE PATTERN/FORM THEY WERE SUPPOSED TO. SOME ALSO APPEARED TO BE A BIT CROOKED AS WELL. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18335373 ↗
• MalfunctionMay 1, 2019Material Twisted/Bent

  IT WAS REPORTED THAT DEVICES HAVE PLASTIC COATING CHIPPING OFF, SOME HAVE THE TIPS BENT AND SOME DO NOT HOLD CLIPS. THERE IS NO ADDITIONAL INFORMATION. NO PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8569012 ↗