QUICKSET 2440-00-555Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 55mm · 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 reamer attachment used in surgery. Most of its 1,066 reports describe the grater failing to cut, and some describe parts that are too dull, chipped or bent. The reports include no deaths and no 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
- 1,065
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,065 adverse event reports that list this exact device (DI 10603295124023), received between Aug 4, 2017 and May 20, 2026 — classified as 1,065 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (792 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 Cut792
- Naturally Worn141
- Dull, Blunt136
- Corroded49
- No Apparent Adverse Event41
- Break34
- Material Twisted/Bent31
- Material Deformation16
Patient problems
- No Clinical Signs, Symptoms or Conditions834
- No Consequences Or Impact To Patient177
- Insufficient Information45
- No Information22
- No Code Available18
- Not Applicable5
Recent adverse event reports
The 25 most recent of 1,065 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 20, 2026Device-Device Incompatibility; Material Deformation; Illegible Information
IT WAS REPORTED THAT REAMER IS BENT. IT WON'T GO ON THE REAMER HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25233209 ↗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 24837784 ↗MalfunctionApr 3, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24776936 ↗MalfunctionApr 3, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24776928 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762618 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762616 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762615 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762613 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762610 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762607 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762605 ↗MalfunctionApr 2, 2026Break
DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762604 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT THE ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24234343 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT THE ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24234055 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT THE ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24234048 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT THE ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24234036 ↗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 24200334 ↗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 24200313 ↗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 24200271 ↗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 24200268 ↗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 24199588 ↗MalfunctionOct 27, 2025Break; Break
IT WAS REPORTED THAT REAMER BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23389650 ↗MalfunctionJul 18, 2025Corroded; Corroded
IT WAS REPORTED THAT THE INSTRUMENT WAS RUSTED OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22541641 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT SURGERY DID NOT HAPPEN IN OLD PINNACLE GRATERS AND THEY NEED REPLACING. DOCTORS ARE COMPLAINING OF BEING VERY DULL AS WELL AS STERILE PROCESSING COMPLAINTS OF RUST AND WARPING. THE INSTRUMENTS ARE OVER 10 YEARS OLD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22514363 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT SURGERY DID NOT HAPPEN IN OLD PINNACLE GRATERS AND THEY NEED REPLACING. DOCTORS ARE COMPLAINING OF BEING VERY DULL AS WELL AS STERILE PROCESSING COMPLAINTS OF RUST AND WARPING. THE INSTRUMENTS ARE OVER 10 YEARS OLD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22514297 ↗
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 2440-00-557Depuy (Ireland) · REAMER1,031 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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