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CLICKLINE 33310DYRecalls & reported problems

Karl Storz GmbH & Co. KG · CLICKLINE Forceps 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 04048551134207), received between Aug 18, 2022 and Aug 18, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 18, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    PER SALESREP WHO WAS NOTIFIED BY THE FACILITY, THAT DURING A PROCEDURE THE DOCTOR WAS REMOVING A SPONGE USING A GRASPER. THE DOCTOR QUESTIONED THE REP REGARDING THE JAW OF THE GRASPER IF A PIN WAS PART OF THE DESIGN. NO FURTHER INFORMATION HAS BEEN PROVIDED BY THE FACILITY IF A PIN FROM THE JAW WAS MISSING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15250716 ↗

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Sources and updates

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