NA 9626-29-000Recalls & reported problems
Depuy International Ltd · ACETABULAR PREPERATION DRILL (HUDSON FITTING) · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy acetabular preparation drill is used to prepare the hip socket during surgery. The 41 reports mostly describe it failing to cut or becoming blunt, breaking or bending, and occasionally jamming; some reports mention broken sleeves or missing parts. There were no deaths or injuries, and 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
- 41
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 41 adverse event reports that list this exact device (DI 10603295243526), received between Jun 9, 2020 and Mar 26, 2026 — classified as 41 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (26 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
- Failure to Cut26
- Break9
- Naturally Worn5
- Material Twisted/Bent3
- Device-Device Incompatibility2
- Material Deformation1
- Material Integrity Problem1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions40
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 25 most recent of 41 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 26, 2026Break
IT WAS REPORTED THAT A SHEATH OF A MARATHON TRAY FROM THE STEP DRILL WAS BROKEN. IT IS SNAPPED INTO TWO PIECES. NO PATIENT HARM, NO DELAYS. ALL PIECES ARE RETRIEVED. DEVICE HAS BEEN DISCARDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24702274 ↗MalfunctionSep 15, 2025Break; Break
THE SLEEVE IS BROKEN ON THE ACETABULAR PREP DRILL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23051648 ↗MalfunctionJan 31, 2025Break; Break
IT WAS REPORTED THAT SEVERAL INSTRUMENTS WERE DAMAGED. THE MEDIUM SIZE DRILL BROKE INTO TWO PIECES DURING USE. THE ACETABULAR CUTTERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21284139 ↗MalfunctionOct 30, 2024Break; Break
IT WAS REPORTED THAT SLEEVES ARE BROKEN. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20571342 ↗MalfunctionOct 30, 2024Break; Break
IT WAS REPORTED THAT SLEEVES ARE BROKEN. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20571332 ↗MalfunctionOct 23, 2023Break; Break
IT WAS REPORTED THAT THE PREP DRILL IS MISSING SLEEVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17984922 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405835 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS:IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405710 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405584 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS:IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405429 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405372 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405303 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405239 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS:IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17405139 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404904 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
DEVICE REPORT FROM DEPUY SYNTHES UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404836 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404711 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404580 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404506 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404451 ↗MalfunctionJul 27, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR PREP DRILL IS BLUNT DUE TO USAGE AND NEEDS TO BE REPLACED. NO PATIENT CONSEQUENCE OR DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17404441 ↗MalfunctionJul 25, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILL IS BLUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17390651 ↗MalfunctionJul 25, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILL IS BLUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17390637 ↗MalfunctionJul 25, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILL IS BLUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17390632 ↗MalfunctionJul 25, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILL IS BLUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17390628 ↗
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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