LIGACLIP LT102Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705036012795), received between Jan 12, 2026 and Jan 12, 2026 — classified as 1 malfunction.

3 other recalls cover devices cleared under the same FDA submission (K830503); they may or may not involve this specific model.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 12, 2026Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE THERE WAS HEMOCLIP ISSUE, IT WAS DEPLOYED WHILE TRYING TO CONTROL THE ACTUAL VESSEL. NO PATIENT CONSEQUENCE HAS BEEN REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24044815 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K830503. One submission often covers many models, so check the product and lot details in each record.

• Z-1777-2013 · Apr 12, 2013 · Terminated
  LIGACLIP Endoscopic Rotating Multiple Clip Applier (ER320), 10mm M/L, bulk non-sterile Product Usage: The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a single patient us
• Z-1775-2013 · Apr 12, 2013 · Terminated
  LIGACLIP Endoscopic Rotating Multiple Clip Applier (ER320), 10mm M/L Product Usage: The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a sterile, single patient use instru
• Z-1776-2013 · Apr 12, 2013 · Terminated
  LIGACLIP Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex Trays), 10mm M/L Product Usage: The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a sterile, sing