LCS 2366-83-000Recalls & reported problems
Depuy (Ireland) · LCS HIP DRILL 45 DEGREES ANGLE · Class 1
Quick summary
This DePuy LCS angled hip drill has 205 malfunction reports, with no deaths and no injuries. Many reports describe the drill tip or bit breaking off or not staying in the driver, and some describe parts not fitting together. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 207
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 207 adverse event reports that list this exact device (DI 10603295120179), received between Jul 21, 2017 and Sep 22, 2026 — classified as 207 malfunctions.
The most frequently reported specific device problem is “Break” (96 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.
Reports received per month
Most reported problems
Device problems
- Break96
- Device-Device Incompatibility64
- Mechanical Jam36
- Naturally Worn14
- Physical Resistance/Sticking9
- Material Deformation6
- Appropriate Device Problem Term/Code Not Available5
- Difficult to Advance3
Patient problems
- No Clinical Signs, Symptoms or Conditions130
- No Consequences Or Impact To Patient49
- Insufficient Information20
- No Information6
- No Code Available5
- Not Applicable1
Recent adverse event reports
The 25 most recent of 207 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Break
It was reported that the angled drills were broken.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50855385 ↗MalfunctionSep 22, 2026Break
It was reported that the angled drills were broken.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50855384 ↗MalfunctionAug 21, 2026No Apparent Adverse Event
It was reported that the instrument had unknown allegation. It did not happen in surgery.Upon manufacturers investigation it was noted that instrument was deformed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50373502 ↗MalfunctionJun 12, 2026Device-Device Incompatibility; Unintended Movement
IT WAS REPORTED THAT THE DRILL HAS LOOSENED AND NO LONGER HOLDS A DRILL BIT PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25486196 ↗MalfunctionMay 19, 2026Break
THE TOP SLIDE PIECE WAS BROKEN OFF COMPLETELY. 45 DEG ANGLE DRILL (236683000) : SIDE AFFECTED: NOT APPLICABLE ## REASON PRODUCT IS NOT AVAILABLE: AVAILABLE. 45 DEG ANGLE DRILL (236683000) : LOT/BATCH NUMBER: [REDACTED]. WAS THERE ANY REPORTED PATIENT OR USER HARM? NO . WAS THERE A SIGNIFICANT DELAY? NO.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25221624 ↗MalfunctionApr 21, 2026Break
IT WAS REPORTED THAT WHEN THE TRAY WAS OPENED IT WAS OBSERVED THAT THE TIP WAS BROKEN OFF, NO OTHER INFORMATION AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24942560 ↗MalfunctionApr 13, 2026Break
IT WAS REPORTED THAT TIP OF DRILL POPPED OFF WHILE DRILLING FOR SCREWS. THROWN AWAY AND REQUESTED A NEW ONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24862239 ↗MalfunctionApr 10, 2026Break
IT WAS REPORTED THAT INSERTER TIP FOR ENDURANCE WAS BENT. STRAIGHT REAMER SHAFT WAS WOBBLING. LPS STEM INSERTER WAS BROKEN. THE 45 DEGREE ANGLE DRILL WAS BROKEN. IT DID NOT HAPPENED IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24843484 ↗MalfunctionApr 10, 2026Break
IT WAS REPORTED THAT THE DRILL BIT WAS BROKE INSIDE DRILL, AND THERE WAS NO PATIENT INVOLVEMENT RELATED TO THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24839630 ↗MalfunctionMar 24, 2026Break; Difficult to Advance
IT WAS REPORTED THAT 45 DEG DRILL IS BROKEN. DRILL BIT WILL NOT SEAT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24675873 ↗MalfunctionMar 19, 2026Break
IT WAS REPORTED THAT THE DRILL SHAFT WAS BROKEN. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24637015 ↗MalfunctionMar 19, 2026Break
IT WAS REPORTED THAT THE DRILL SHAFT WAS BROKEN. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24637013 ↗MalfunctionMar 16, 2026Break
IT WAS REPORTED THAT THE INSTRUMENT WAS FOUND BROKEN WHEN THE TRAY WAS OPENED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24604030 ↗MalfunctionMar 11, 2026Break
IT WAS REPORTED THAT THE INSTRUMENT BROKE DURING THE TOTAL HIP PROCEDURE. SURGEON HAD BACKUPS, SO THERE WAS NO DELAY TO SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24576018 ↗MalfunctionJan 23, 2026Break
IT WAS REPORTED THAT DURALOC DRILL AND ALSO T HANDLE BROKE DURING TOTAL HIP. T HANDLE WHITE HANDLE CRACKED, AND DURALOC DRILL PIECE THAT HOLDS DRILL BIT ALSO BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24159633 ↗MalfunctionDec 19, 2025Break; Break
IT WAS REPORTED THAT THE DURALOC ANGLED DRILL BROKEN. REQUIRED REPLACEMENT ASAP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23850408 ↗MalfunctionDec 19, 2025Break; Break
IT WAS REPORTED THAT THE DURALOC ANGLED DRILL WAS BROKEN. REQUIRED REPLACEMENT ASAP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23850273 ↗MalfunctionDec 3, 2025Break; Break
IT WAS REPORTED THAT AFTER THE SURGERY WHILE REASSEMBLING TRAYS IN STERILE PROCESSING DEPARTMENT THE DRILL DRIVER SHAFT CAME APART. ALL PARTS ARE ACCOUNTED FOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23705176 ↗MalfunctionNov 10, 2025Break; Break
IT WAS REPORTED THAT WHILE USING THE FIXED ANGLED DRILL SHAFT THE CENTER PIECE THAT HOLDS THE MODULAR DRILL BIT BROKE OFF. ALL PIECES WERE RECOVERED NO PATIENT HARM OR ADDED TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23510720 ↗MalfunctionAug 29, 2025Break; Break
IT WAS REPORTED THAT THE GUIDE POSTS FOR DRILL BIT ON DRILL ADAPTER PIECE WAS BROKEN/ NOT SECURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22923863 ↗MalfunctionJul 21, 2025Break; Break
IT WAS REPORTED THAT THERE WAS A BROKEN ANGLED DRILL AND DRILL BIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22556001 ↗MalfunctionJul 7, 2025No Apparent Adverse Event; No Apparent Adverse Event
THE ITEM WAS REPORTED FOR UNKNOWN REASON. THE EVENT DID NOT HAPPENED DURING A SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22414143 ↗MalfunctionJun 30, 2025Break; Break
IT WAS REPORTED THAT THE INSTRUMENT WAS BROKEN. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22358462 ↗MalfunctionJun 27, 2025Break; Break
IT WAS REPORTED THAT WHEN THE DOCTOR WAS DRILLING FOR SCREWS DURING A TOTAL HIP REPLACEMENT, THE END PART OF THE DRILL BROKE OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22344574 ↗MalfunctionJun 25, 2025Difficult to Advance; Difficult to Advance
IT WAS REPORTED THAT PATIENT UNDERWENT TOTAL HIP REPLACEMENT ON (B)(6) 2025. WHILE THE SURGEON WAS USING THE DRILL SHAFT, EVERY DRILL BIT THAT WAS PLACED IN THERE WAS WOBBLING. THE CONNECTOR WOULD NOT ALLOW THE DRILL BIT TO ADVANCE STRAIGHT INTO THE PELVIS. THE WAS NO SURGICAL DELAY AND ALL PIECES WERE RECOVERED FROM THE FIELD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22332182 ↗
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
- QUICKSET 2274-52-000Depuy (Ireland) · BIT, DRILL186 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.