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LIGACLIP LX220Recalls & reported problems

Ethicon Endo-Surgery, LLC · Ligaclip Clip Applier Medium Angled Jaw 26.7cm · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20705036012914), received between Jun 9, 2020 and Jun 9, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Form Staple” (1 report).

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

Device problems

  • Failure to Form Staple1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJun 9, 2020Failure to Form Staple; Failure to Form Staple

    IT WAS REPORTED THAT DURING A FIBROID LOBECTOMY THE CLIPS WERE NOT FOLDING EVENLY AND NOT CLAMPING FULLY. SOME OF THE CLIPS FELL OUT OF THE JAW. THE CLIPS DID NOT FALL INTO THE PATIENT. THE PROCEDURE WAS COMPLETED WITH THIS SAME DEVICE WITH NO PATIENT CONSEQUENCES REPORTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10135391 ↗

Other Applier, surgical, clip devices

All Applier, surgical, clip devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.