QUICKSET 2274-54-500Recalls & reported problems
Depuy Orthopaedics, Inc. · QUICKSET DRILL GUIDE II 3.8mm · Class 1
All models of QUICKSET (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy QuickSet drill guide is a surgical template used to help guide drill bits during hip surgery. The 49 reports mostly describe the guide breaking, warping or bending, and drill bits getting stuck or snapping inside it, sometimes leaving fragments that were removed, plus heat at the site and trouble fitting other instruments around it. No deaths or injuries are reported. There are 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
- 49
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 49 adverse event reports that list this exact device (DI 10603295109297), received between Jun 29, 2017 and Apr 6, 2026 — classified as 49 malfunctions.
The most frequently reported specific device problem is “Break” (22 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
- Break22
- Device-Device Incompatibility16
- Material Deformation15
- Appropriate Device Problem Term/Code Not Available2
- Material Twisted/Bent2
- Corroded1
- Dull, Blunt1
- Illegible Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions28
- No Consequences Or Impact To Patient12
- Insufficient Information6
- No Code Available3
- No Information1
- Not Applicable1
Recent adverse event reports
The 25 most recent of 49 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2026Device-Device Incompatibility
IT WAS REPORTED THAT DURING SURGERY SETUP, THE DRILL BIT WOULD NOT FEED THROUGH THE DRILL GUIDE. THE SURGERY WAS NOT DELAYED. IT WAS FURTHER REPORTED THAT THERE WAS NO ISSUE WITH THE DRILL. THE DRILL GUIDE WAS REMOVED AND WAS NO LONGER BEING USED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790361 ↗MalfunctionFeb 4, 2026Device-Device Incompatibility
IT WAS REPORTED THAT THE DRILL BIT BENT AND GOT STUCK IN DRILL GUIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24257800 ↗MalfunctionNov 6, 2025Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THE CAPTURE DEVICE WOULD NOT FIT AROUND THE DRILL BIT AS IT WAS DEFORMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23489997 ↗MalfunctionOct 16, 2025Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED THAT PATIENT UNDERWENT HIP SURGERY ON (B)(6) 2025. THE DRILL GUIDE WAS USED FOR SCREWS IN THE ACETABULAR SHELL AND DRILL BITS KEPT BREAKING. THE GUIDE WAS ALSO GETTING HOT. SURGEON THINKS THE DRILL BITS WERE HITTING ON THE DRILL GUIDE BECAUSE IT WAS WARPED. FRAGMENTS WERE GENERATED BUT ALL REMOVED. NEW DRILL BITS WERE USED. DRILL BITS WERE THROWN OUT BUT NOT THE DRILL GUIDE. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO DELAY. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23315827 ↗MalfunctionMay 30, 2025Device-Device Incompatibility; Device-Device Incompatibility
DRILL BIT GOT STUCK/BINDED IN THE QUICKSET DRILL GUIDE. IT WAS THOUGHT THAT THE QUICKSET DRILL GUIDE WAS DEFECTIVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22112960 ↗MalfunctionMar 7, 2025Break; Break
IT WAS REPORTED THAT THE DRILL GUIDE BROKE DURING CLEANING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21547996 ↗MalfunctionFeb 5, 2025Incorrect Measurement; Incorrect Measurement
IT WAS REPORTED THAT DURING MDRD INSPECTION DEVICE WAS FOUND TO BE NO LONGER SUITABLE FOR USE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21312474 ↗MalfunctionJan 31, 2025Break; Break
IT WAS REPORTED THAT THERE WERE BROKEN INSTRUMENTS. THERE WAS NO PATIENT INVOLVEMENT. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21284330 ↗MalfunctionOct 11, 2024Device-Device Incompatibility; Device-Device Incompatibility
ADDITIONAL INFORMATION WAS RECEIVED AND STATES THAT: A. WERE THERE ANY ADVERSE CONSEQUENCE/S THAT AFFECTED THE PATIENT BECAUSE OF THE REPORTED EVENT? - NONE REPORTED. B. CAN YOU PROVIDE THE LOT NUMBER OF THE REPORTED PRODUCT? ¿ LOT NUMBER WAS UNREADABLE.
Patient problems: Insufficient Information
MAUDE report 20433170 ↗MalfunctionAug 27, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT THE INSTRUMENT WAS BENT. IT WAS UNKNOWN, IF THERE WAS A SURGICAL DELAY.
Patient problems: Insufficient Information
MAUDE report 20078904 ↗MalfunctionJul 9, 2024Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THE DRILL GUIDE WAS WARPED AND DRILL BIT COULD NOT PASS THROUGH IT. IT WAS THROWN AWAY IN CASE. IT WAS NOT ABLE TO RETURN.
Patient problems: Insufficient Information
MAUDE report 19699969 ↗MalfunctionMar 15, 2024Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE DRILL DOES NOT FIT IN THE GUIDE.
Patient problems: Insufficient Information
MAUDE report 18911617 ↗MalfunctionFeb 27, 2024Device-Device Incompatibility; Device-Device Incompatibility
THE EVENT DID NOT HAPPEN IN SURGERY, DRILLS WILL NOT FIT INSIDE DRILL GUIDE.
Patient problems: Insufficient Information
MAUDE report 18787816 ↗MalfunctionJan 3, 2024Device-Device Incompatibility; Material Deformation; Illegible Information; Device-Device Incompatibility; Material Deformation; Illegible Information
IT WAS REPORTED THE DRILL WOULD NOT EASILY GLIDE THROUGH THE GUIDE. UPON FURTHER EXAMINATION IT LOOKED AS IF THE DRILL GUIDE HAD BECOME BENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18434729 ↗MalfunctionDec 13, 2023Material Deformation; Material Deformation
IT WAS REPORTED THAT THE DRILL GUIDE BENT. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18323033 ↗MalfunctionNov 17, 2023Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT DRILL GUIDE WAS BENT SO THAT IT WOULD NOT FIT OVER THE DRILL BIT.
Patient problems: Insufficient Information
MAUDE report 18158427 ↗MalfunctionSep 15, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE DRILL GUIDE AND DRILL BIT JAMMED TOGETHER AND UNABLE TO SEPARATE. WAS SURGERY DELAYED DUE TO THE REPORTED EVENT? NO, WAS PROCEDURE SUCCESSFULLY COMPLETED? YES, WERE FRAGMENTS GENERATED? NO, IF YES, WERE THEY REMOVED EASILY WITHOUT ADDITIONAL INTERVENTION? UNKNOWN, PATIENT STATUS/ OUTCOME / CONSEQUENCES NO, WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED: UNKNOWN, IS THE PATIENT PART OF A CLINICAL STUDY UNKNOWN, (B)(4) DEVICE PROPERTY OF: NONE, DEVICE IN POSSESSION OF: NONE, (B)(4) DEVICE PROPERTY OF: NONE, DEVICE IN POSSESSION OF: NONE. BY CHECKING THIS BOX I CERTIFY THAT ALL INFORMATION THAT ARE KNOWN/AVAILABLE HAS BEEN DISCLOSED. IF ANY NEW INFORMATION WILL BE MADE AVAILABLE, THE ADDITIONAL INFORMATION WILL BE SUBMITTED THROUGH CST. TRUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17757080 ↗MalfunctionAug 30, 2023Break; Break
IT WAS REPORTED THAT 35MM DRILL BIT BROKE WHILE DRILLING FOR A SCREW - THE DRILL BIT DID NOT NEED TO BE PULLED FROM THE BODY BECAUSE IT WAS STUCK IN THE DRILL GUIDE. THE BROKEN BIT WAS SUBSEQUENTLY PULLED OUT OF THE DRILL GUIDE AND THE SURGERY PROCEEDED WITHOUT INCIDENT. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17650221 ↗MalfunctionAug 22, 2023Break; Break
IT WAS REPORTED THAT DEVICE WAS BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17597436 ↗MalfunctionJul 10, 2023Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
PINNACLE FLEXIBLE DRILL BIT AND DRILL GUIDE BECAME ENTANGLED DURING USE. THEY KINKED UP AND BECOME INEFFECTIVE AND UNUSABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17287096 ↗MalfunctionApr 20, 2023Material Deformation; Material Deformation
IT WAS REPORTED THAT DRILL GUIDE IS BENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16775711 ↗MalfunctionApr 19, 2023Break; Break
IT WAS REPORTED THE INSTRUMENT BROKE DURING SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16773885 ↗MalfunctionMar 29, 2023Break; Break
IT WAS REPORTED THAT THE INSTRUMENTS WERE BROKEN IN SPD. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16636798 ↗MalfunctionOct 13, 2022Break; Break
IT WAS REPORTED THAT THE ITEM IS BROKEN - NO FURTHER INFORMATION AVAILABLE FROM CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15594582 ↗MalfunctionOct 7, 2022Break; Break
IT WAS REPORTED THAT THE DRILL GUIDE BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15564598 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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.
How reports and recalls are matched · Editorial policy · Report an error on this page