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
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
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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