QUICKSET 2440-00-560Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 60mm · 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 reamer used during joint replacement surgery. Its 457 reports mostly describe the grater failing to cut, along with corrosion, dull or chipped edges, and breakage. There are 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
- 457
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 457 adverse event reports that list this exact device (DI 10603295124078), received between Sep 21, 2017 and May 21, 2026 — classified as 457 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (309 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 Cut309
- Corroded61
- Naturally Worn44
- Dull, Blunt40
- No Apparent Adverse Event31
- Break23
- Adverse Event Without Identified Device or Use Problem13
- Material Deformation11
Patient problems
- No Clinical Signs, Symptoms or Conditions365
- No Consequences Or Impact To Patient69
- Insufficient Information19
- No Information5
- No Code Available4
- Not Applicable3
Recent adverse event reports
The 25 most recent of 457 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2026Break
IT WAS REPORTED THAT THE REAMER GRATER CONNECTION HAD BROKEN. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25242435 ↗MalfunctionApr 9, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. NO OTHER INFORMATION WAS PROVIDED AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24837650 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791336 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791305 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791248 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791205 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791174 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791161 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791139 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790880 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790851 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790833 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790804 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790778 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790767 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790760 ↗MalfunctionFeb 2, 2026Failure to Cut
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24235618 ↗MalfunctionFeb 2, 2026Failure to Cut
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24235304 ↗MalfunctionFeb 2, 2026Failure to Cut
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24235271 ↗MalfunctionFeb 2, 2026Failure to Cut
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24235173 ↗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 24201974 ↗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 24201964 ↗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 24201962 ↗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 24201891 ↗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 24201869 ↗
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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