NA ETHMCM20Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888551019064), received between Dec 17, 2021 and Dec 17, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Failure to Fire” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 17, 2021Failure to Fire; Mechanical Jam; Failure to Fire; Mechanical Jam

  IT WAS REPORTED THAT A (B)(6) MALE PATIENT UNDERWENT A LAPAROSCOPIC OPEN CHOLECYSTECTOMY PROCEDURE WITH FOUR REPROCESSED CLIP APPLIERS LIGACLIP AND, DURING THE PROCEDURE, THE FOUR CLIP APPLIERS FAILED TO FIRE. A FIFTH CLIP WAS USED AND WORKED AS EXPECTED. THERE WAS NO PATIENT CONSEQUENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13025831 ↗
• MalfunctionDec 17, 2021Failure to Fire; Mechanical Jam; Failure to Fire; Mechanical Jam

  IT WAS REPORTED THAT A (B)(6), MALE, PATIENT UNDERWENT A LAPAROSCOPIC OPEN CHOLECYSTECTOMY PROCEDURE WITH FOUR REPROCESSED CLIP APPLIERS LIGACLIP AND DURING THE PROCEDURE, THE FOUR CLIP APPLIERS FAILED TO FIRE. A FIFTH CLIP WAS USED AND WORKED AS EXPECTED. THERE WAS NO PATIENT CONSEQUENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13025791 ↗