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CLICKLINE 34310MSRecalls & reported problems

Karl Storz GmbH & Co. KG · CLICKLINE Scissors Insert · Class 2

All models of CLICKLINE (46)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 04048551152980), received between May 22, 2019 and May 22, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Integrity Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Material Integrity Problem1
  • Material Perforation1

Patient problems

  • Patient Problem/Medical Problem1

Recent adverse event reports

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

  • MalfunctionMay 22, 2019Material Perforation; Material Integrity Problem; Material Perforation; Material Integrity Problem

    ALLEGEDLY, DURING AN APPENDECTOMY PROCEDURE, WHILE THE DOCTOR WAS CAUTERIZING INSIDE, HE WAS TOO CLOSE TO THE BOWEL AND HIT IT BUT DID NOT PERFORATE THE BOWEL.

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 8632282 ↗

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Sources and updates

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