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QUICKSET 2274-59-000Recalls & reported problems

Depuy (Ireland) · QUICKSET 3.8mm DIA DRILL BIT 70mm · Class 1

All models of QUICKSET (66)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
18
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 10603295109341), received between Oct 19, 2017 and Jul 17, 2025 — classified as 18 malfunctions.

The most frequently reported specific device problem is “Break” (11 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 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 3 reportsJun 2025: 2 reportsJul 2025: 3 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break11
  • Naturally Worn3
  • Dull, Blunt2
  • Material Deformation2
  • Failure to Cut1

Patient problems

  • No Clinical Signs, Symptoms or Conditions13
  • Insufficient Information2
  • No Code Available1
  • No Information1
  • No Known Impact Or Consequence To Patient1
  • Not Applicable1

Recent adverse event reports

The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 17, 2025Break; Break

    IT WAS REPORTED THAT THERE WAS BREAKAGE AND REPAIR OF CONSIGNED ITEMS IN THE ACCOUNT FROM GENERAL USAGE. NO OTHER INFORMATION WAS PROVIDED AT THIS TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22532340 ↗
  • MalfunctionJul 17, 2025Break; Break

    IT WAS REPORTED THE DEVICES WERE BROKEN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22532159 ↗
  • MalfunctionJul 17, 2025Break; Break

    IT WAS REPORTED THE DEVICES WERE BROKEN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22532149 ↗
  • MalfunctionJun 9, 2025Break; Break

    IT WAS REPORTED THAT THE DRILL BITS SNAPPED OVER TIME WHEN DRILLING BONE.

    Patient problems: Insufficient Information

    MAUDE report 22167023 ↗
  • MalfunctionJun 9, 2025Break; Break

    IT WAS REPORTED THAT THE DRILL BITS SNAPPED OVER TIME WHEN DRILLING BONE.

    Patient problems: Insufficient Information

    MAUDE report 22167022 ↗
  • MalfunctionMay 15, 2025Break; Break

    IT WAS REPORTED MULTIPLE DRILL BITS HAVE BROKEN OFF OVER MANY MONTHS. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22028080 ↗
  • MalfunctionMay 15, 2025Break; Break

    IT WAS REPORTED MULTIPLE DRILL BITS HAVE BROKEN OFF OVER MANY MONTHS. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22027748 ↗
  • MalfunctionMay 15, 2025Break; Break

    IT WAS REPORTED MULTIPLE DRILL BITS HAVE BROKEN OFF OVER MANY MONTHS. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22027079 ↗
  • MalfunctionOct 3, 2022Break; Break

    IT WAS REPORTED THAT THE QUICKSET 70 MM DRILL BIT SNAPPED IN HALF DURING PROCEDURE. THE TWO BROKEN PIECES WERE COLLECTED AND REMOVED FROM THE BODY. THERE WAS NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15532230 ↗
  • MalfunctionFeb 10, 2022Naturally Worn; Naturally Worn

    THEY HAVE ALL WORN OVER TIME AND NEED REPLACING. THERE WAS NO IMPACT ON SURGERY OR PATIENT. NOTIFICATION DATE: 03.02.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13510866 ↗
  • MalfunctionFeb 10, 2022Naturally Worn; Naturally Worn

    THEY HAVE ALL WORN OVER TIME AND NEED REPLACING. THERE WAS NO IMPACT ON SURGERY OR PATIENT. NOTIFICATION DATE: 03.02.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13510862 ↗
  • MalfunctionDec 1, 2021Material Deformation; Material Deformation

    IT WAS REPORTED THAT THE DRILL BITS HAVE BECOME BENT OVER TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12909018 ↗
  • MalfunctionDec 1, 2021Material Deformation; Material Deformation

    IT WAS REPORTED THAT THE DRILLS HAVE BECOME BENT OVER TIME SO ARE NO LONGER SAFE TO USE ON THE SET.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12908673 ↗
  • MalfunctionJul 22, 2021Failure to Cut; Failure to Cut

    IT WAS REPORTED THAT THE DRILL BITS ON THE SET WERE BLUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12210411 ↗
  • MalfunctionApr 14, 2021Break; Break

    DRILL BITS BROKEN AND REQUIRING REPLACEMENT ON KIT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11667446 ↗
  • MalfunctionJun 25, 2020Dull, Blunt; Dull, Blunt

    THE SURGEON; PORT MACQUARIE BASE HOSPITAL (B)(6) 2020; TWO DRILL BITS BROKEN USING CASE ALSO DRILL BITS BLUNT. ACTION TAKEN TO MANAGE THE ISSUE: SINGLE USE SMITH AND NEPHEW DRILL BIT USED - COMPETITOR SINGLE USE PRODUCT USED. 10 MINUTE DELAY TO THE PROCEDURE, NO AE TO PATIENT.

    Patient problems: No Code Available; Not Applicable

    MAUDE report 10193301 ↗
  • MalfunctionOct 8, 2018Break; Break

    PINNACLE/CORAIL HIP REPLACEMENT; A MALONE, (B)(6) HOSPITAL, (B)(6) 2018. DURING THE OPERATION A SCREW WAS REQUIRED, WHEN DRILLING FOR A SCREW THE DRILL BIT BROKE, ALL PARTS APPEAR TO HAVE BEEN REMOVED FROM THE PATIENT, THE PROCEDURE WAS FINISHED WITH A SHORTER DRILL FROM THE SET. PATIENT APPEARS TO BE OK. 1 MINUTE DELAY TO THE PROCEDURE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7942251 ↗
  • MalfunctionOct 19, 2017Dull, Blunt; Naturally Worn; Dull, Blunt; Naturally Worn

    IT WAS REPORTED THAT THE DRILL BITS WERE NOTED TO BE BLUNT.

    Patient problems: No Information

    MAUDE report 6960794 ↗

Other BIT, DRILL devices

All BIT, DRILL devices →

Sources and updates

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