Click'X 388.353Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034772516), received between Jan 31, 2022 and Aug 2, 2022 — classified as 2 malfunctions.

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

• MalfunctionAug 2, 2022Material Integrity Problem; Material Integrity Problem

  DEVICE REPORT FROM THE NETHERLANDS REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT (B)(6) 2022, THE EXTRACTION PLIERS WERE DISCOVERED TO BE CORRODED AND A PIECE WAS BROKEN OFF. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT. THIS REPORT IS FOR AN EXTRACTION PLIERS FOR CLICK'X. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15149893 ↗
• MalfunctionJan 31, 2022Material Integrity Problem; Material Integrity Problem

  IT WAS REPORTED ON (B)(6) 2022, THE EXTRACTION PLIERS WAS FOUND TO BE BROKEN DURING THE PREOP INSPECTION. NO PATIENT INVOLVEMENT. THIS REPORT IS FOR ONE (1) EXTRACTION PLIERS FOR CLICK'X. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13402639 ↗