QUICKSET 2440-00-554Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 54mm · Class 1
All models of QUICKSET (66)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy QuickSet grater head is an orthopedic reamer. Most of the 840 reports describe the grater failing to cut, and many mention dullness, wear, corrosion or breakage. The reports record no injuries and no deaths. 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
- 840
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 840 adverse event reports that list this exact device (DI 10603295124016), received between Aug 16, 2017 and Apr 27, 2026 — classified as 840 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (606 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Cut606
- Dull, Blunt129
- Naturally Worn115
- No Apparent Adverse Event43
- Corroded41
- Break31
- Material Twisted/Bent15
- Material Deformation10
Patient problems
- No Clinical Signs, Symptoms or Conditions632
- No Consequences Or Impact To Patient156
- Insufficient Information44
- No Information22
- No Code Available10
- Not Applicable6
Recent adverse event reports
The 25 most recent of 840 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 27, 2026Break
IT WAS REPORTED THAT DURING STERILE REPROCESSING IT WAS OBSERVED THAT THE TEETH ON QUICKSET ACE GRATER HEAD 54MM DEVICE HAD BECOME DULL AND CHIPPED. IT WAS FURTHER OBSERVED THAT THE PIN TRL LNR +4 NEUT 540DX32ID DEVICE WAS CRACKED AND CHIPPED. THESE ITEMS WERE DEEMED TO BE NO LONGER FUNCTIONAL AND WERE SUBSEQUENTLY DISCARDED. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT, OR SURGICAL DELAY REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25008944 ↗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 24762834 ↗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 24762830 ↗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 24762829 ↗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 24762827 ↗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 24762825 ↗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 24762824 ↗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 24762823 ↗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 24762814 ↗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 24762804 ↗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 24762803 ↗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 24234057 ↗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 24234050 ↗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 24233928 ↗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 24233881 ↗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 24198273 ↗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 24198271 ↗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 24198266 ↗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 24198256 ↗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 24198228 ↗MalfunctionNov 12, 2025Break; Break
IT WAS REPORTED THAT THE 54MM QUICKSET GRATER BROKE DURING ACETABULAR REAMING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23536123 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEEDED TO BE REPLACED. DOCTORS COMPLAINED THAT THEY WERE VERY DULL AND STERILE PROCESSING COMPLAINED OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22506893 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEEDED TO BE REPLACED. DOCTORS COMPLAINED THAT THEY WERE VERY DULL AND STERILE PROCESSING COMPLAINED OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22506817 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEEDED TO BE REPLACED. DOCTORS COMPLAINED THAT THEY WERE VERY DULL AND STERILE PROCESSING COMPLAINED OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22506816 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEEDED TO BE REPLACED. DOCTORS COMPLAINED THAT THEY WERE VERY DULL AND STERILE PROCESSING COMPLAINED OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22506815 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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