QUICKSET 2440-00-559Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 59mm · 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 has 695 adverse event reports, with no deaths and no injuries. Most describe the grater failing to cut, and some reports say staff found the graters too dull and chipped to use on a patient during reprocessing. 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
- 696
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 696 adverse event reports that list this exact device (DI 10603295124061), received between Sep 19, 2017 and Sep 25, 2026 — classified as 696 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (517 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 Cut517
- Naturally Worn69
- Corroded58
- Dull, Blunt48
- Break29
- No Apparent Adverse Event28
- Adverse Event Without Identified Device or Use Problem18
- Material Twisted/Bent18
Patient problems
- No Clinical Signs, Symptoms or Conditions570
- No Consequences Or Impact To Patient88
- Insufficient Information32
- No Information8
- No Code Available7
- Not Applicable6
Recent adverse event reports
The 25 most recent of 696 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Break
It was reported that reamer basket broke. There was no delay to the procedure. There were no adverse events. All parts were retrieved.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898514 ↗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 24837658 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790907 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790896 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790716 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790537 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790529 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790514 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790504 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790502 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790493 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790486 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790481 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790470 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790464 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790176 ↗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 24235601 ↗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 24235461 ↗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 24235317 ↗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 24235313 ↗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 24201799 ↗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 24201778 ↗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 24201766 ↗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 24201759 ↗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 24201741 ↗
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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