Skip to content

LEVEL ONE 25-472-75-07Recalls & reported problems

KLS-Martin L.P. · TWIST DRILL, J NOTCH, MORRISON, 25 MM STOP, FOR 25-471-05-07 · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888118041432), received between Sep 28, 2018 and Jan 4, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Temperature 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Temperature Problem2
  • Use of Device Problem1

Patient problems

  • Burn(s)2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 4, 2019Temperature Problem; Temperature Problem

    IT WAS REPORTED A PATIENT WAS BURNED WHILE USING A TWIST DRILL AND TROCAR.

    Patient problems: Burn(s)

    MAUDE report 8217430 ↗
  • InjurySep 28, 2018Use of Device Problem; Temperature Problem; Use of Device Problem; Temperature Problem

    IT WAS REPORTED A PATIENT WAS BURNED WHILE USING A TWIST DRILL AND TROCAR. THE TWIST DRILL WAS BEING USED AT 20,000 RMPS. IT IS STATED IN IFU 90-274-92-40 "TWIST DRILLS ARE NOT DESIGNED TO BE USED AT SPEEDS IN EXCESS OF 5000 RPM."

    Patient problems: Burn(s)

    MAUDE report 7919303 ↗

Other BIT, DRILL devices

All BIT, DRILL devices →

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