QUICKSET 2440-00-543Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 43mm · Class 1
All models of QUICKSET (66)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy QuickSet grater head is a surgical tool used to shape the hip socket during hip replacement. Its 557 reports mostly describe graters that fail to cut, have grown dull, or show corrosion and wear, and most list no patient effect. The reports include no deaths and no injuries. 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
- 557
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 557 adverse event reports that list this exact device (DI 10603295123903), received between Sep 20, 2017 and Jan 28, 2026 — classified as 557 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (411 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 Cut411
- Naturally Worn71
- Corroded44
- Dull, Blunt44
- Material Twisted/Bent26
- No Apparent Adverse Event23
- Break15
- Adverse Event Without Identified Device or Use Problem8
Patient problems
- No Clinical Signs, Symptoms or Conditions458
- No Consequences Or Impact To Patient64
- Insufficient Information38
- No Information5
- No Code Available4
- Not Applicable4
Recent adverse event reports
The 25 most recent of 557 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM. THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24202048 ↗MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM. THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24197988 ↗MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24197983 ↗MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM. THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24197982 ↗MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM. THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24197976 ↗MalfunctionJul 22, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22565203 ↗MalfunctionJul 22, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22565198 ↗MalfunctionJul 7, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT ITEMS NEED REPLACED WITH CROSS BACKS. A PRODUCT HAS BEEN REPORTED BUT THE REASON FOR REPORTING IS UNKNOWN. THIS EVENT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS FOUND THAT THE CUTTING EDGES OF THE DEVICE ARE BLUNTING/ROUNDING. ADDITIONALLY SIGNS OF CORROSION WERE OBSERVED AROUND THE CUTTING SURFACE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22414004 ↗MalfunctionJun 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS WERE DULL. THERE WAS NO PROCEDURE OR PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22144744 ↗MalfunctionJun 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS WERE DULL. THERE WAS NO PROCEDURE OR PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22144379 ↗MalfunctionMay 14, 2025No Apparent Adverse Event; No Apparent Adverse Event
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 22017698 ↗MalfunctionApr 17, 2025Break; Crack; Material Deformation; Break; Crack; Material Deformation
IT WAS REPORTED THAT THE TECH NOTICED ALL 3 GRATERS HAD THE GRATER CUT OUT BENT INWARD AND WERE DULL, THE OTHER LOOKED TO HAVE A SMALL CRACK ON THE CROSS SECTION ALONG THE BACKSIDE THAT CONNECTS TO HANDLE. THE GRATERS WERE PULLED FROM THAT TRAY. NO ISSUES WITH DELAYS OR ISSUES WITH THE GRATERS USED FOR THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21853931 ↗MalfunctionMar 6, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME WITH REPEATED USE. THE ISSUE DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21541087 ↗MalfunctionMar 6, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME WITH REPEATED USE. THE ISSUE DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21539511 ↗MalfunctionMar 5, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THE GRATERS ARE DULL. NO SURGICAL DELAY. PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21527275 ↗MalfunctionMar 5, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THE GRATERS ARE DULL. NO SURGICAL DELAY. PROCEDURE WAS COMPLETED SUCCESSFULLY
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21526350 ↗MalfunctionMar 5, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THE GRATERS ARE DULL. NO SURGICAL DELAY. PROCEDURE WAS COMPLETED SUCCESSFULLY
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21526261 ↗MalfunctionMar 5, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THE GRATERS ARE DULL. NO SURGICAL DELAY. PROCEDURE WAS COMPLETED SUCCESSFULLY
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21526080 ↗MalfunctionSep 24, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT GRATERS HAVE BECOME DULL AND NEED REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20296850 ↗MalfunctionSep 17, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS HAVE BECOME DULL AND NEED TO BE REPLACED. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20242715 ↗MalfunctionSep 17, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS HAVE BECOME DULL AND NEED TO BE REPLACED. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20242713 ↗MalfunctionSep 10, 2024No Apparent Adverse Event; No Apparent Adverse Event
THE GRATER HEADS WERE REPORTED FOR AN UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 20185647 ↗MalfunctionSep 10, 2024No Apparent Adverse Event; No Apparent Adverse Event
THE GRATER HEADS WERE REPORTED FOR AN UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 20185645 ↗MalfunctionSep 10, 2024No Apparent Adverse Event; No Apparent Adverse Event
THE GRATER HEADS WERE REPORTED, FOR AN UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 20185644 ↗MalfunctionSep 9, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE REAMERS WERE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20176398 ↗
Other REAMER devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 reports
- QUICKSET 2440-00-553Depuy (Ireland) · REAMER1,105 reports
- QUICKSET 2440-00-547Depuy (Ireland) · REAMER1,073 reports
- QUICKSET 2440-00-555Depuy (Ireland) · REAMER1,065 reports
- QUICKSET 2440-00-557Depuy (Ireland) · REAMER1,031 reports
- QUICKSET 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 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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