DURALOC 2244-14-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295107491), received between Feb 8, 2018 and Nov 6, 2025 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 6, 2025Structural Problem; Structural Problem

  IT WAS REPORTED THAT THE INLAY DRUM PLIERS HAD A DEFECT, AND THE TIP OF THE PLIERS NO LONGER GRIPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23487969 ↗
• MalfunctionDec 6, 2021Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE LINER EXTRACTOR WAS NOTED TO BE JAMMED. SURGERY WAS NOT DELAYED. NO PIECES WERE BROKEN OFF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12934930 ↗
• MalfunctionFeb 12, 2019Break; Break

  IT WAS REPORTED THAT THE DURALOC LINER EXTRACTION ARE BROKEN.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8332808 ↗
• MalfunctionFeb 8, 2018Device Issue; Device Issue

  IT WAS REPORTED THAT THE DURALOC POLY EXTRACTOR BROKE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7250821 ↗