QUICKSET 2440-00-557Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 57mm · 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 the subject of 1,031 adverse event reports, which mention no deaths or injuries. Most reports describe the grater failing to cut, along with dull, worn, corroded or broken parts. Some describe cracked handles and clasps that no longer tighten. 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
- 1,031
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,031 adverse event reports that list this exact device (DI 10603295124047), received between Jul 12, 2017 and May 15, 2026 — classified as 1,031 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (763 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 Cut763
- Naturally Worn106
- Dull, Blunt104
- Corroded49
- No Apparent Adverse Event44
- Break37
- Adverse Event Without Identified Device or Use Problem27
- Material Twisted/Bent21
Patient problems
- No Clinical Signs, Symptoms or Conditions822
- No Consequences Or Impact To Patient149
- Insufficient Information50
- No Information23
- No Code Available16
- Not Applicable5
- Foreign Body In Patient1
Recent adverse event reports
The 25 most recent of 1,031 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 15, 2026Material Deformation
IT WAS REPORTED THAT REAMER BAR WAS BENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25186253 ↗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 24837745 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790034 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790030 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790018 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790006 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789883 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789781 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789761 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789743 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789731 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789705 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789699 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789680 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789667 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789663 ↗MalfunctionJan 29, 2026Failure to Cut
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207370 ↗MalfunctionJan 29, 2026Failure to Cut
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207369 ↗MalfunctionJan 29, 2026Failure to Cut
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207368 ↗MalfunctionJan 29, 2026Failure to Cut
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207367 ↗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 24201129 ↗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 24201102 ↗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 24201096 ↗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 24201088 ↗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 24201080 ↗
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 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 reports
- QUICKSET 2440-00-550Depuy (Ireland) · REAMER870 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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