QUICKSET 2440-00-553Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 53mm · 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 1,105 reports describe the grater failing to cut, with staff finding it too dull or chipped during reprocessing. 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
- 1,105
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,105 adverse event reports that list this exact device (DI 10603295124009), received between Jul 11, 2017 and Apr 6, 2026 — classified as 1,105 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (823 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 Cut823
- Dull, Blunt148
- Naturally Worn126
- Corroded47
- No Apparent Adverse Event43
- Material Twisted/Bent37
- Break31
- Material Deformation14
Patient problems
- No Clinical Signs, Symptoms or Conditions852
- No Consequences Or Impact To Patient196
- Insufficient Information49
- No Information23
- No Code Available16
- Not Applicable4
Recent adverse event reports
The 25 most recent of 1,105 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793677 ↗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 24777060 ↗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 24762931 ↗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 24762930 ↗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 24762927 ↗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 24762922 ↗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 24762918 ↗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 24762916 ↗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 24762915 ↗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 24762913 ↗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 24762910 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED THAT THE ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24233718 ↗MalfunctionJan 29, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207503 ↗MalfunctionJan 29, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207501 ↗MalfunctionJan 29, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207495 ↗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 24198254 ↗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 24198251 ↗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 24198237 ↗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 24198234 ↗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 24198196 ↗MalfunctionNov 17, 2025Break; Device-Device Incompatibility; Break; Device-Device Incompatibility
IT WAS REPORTED THAT THE 53MM GRATER HAS BROKEN AND WOULD NOT ATTACH TO THE REAMER HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23575783 ↗MalfunctionJul 18, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS ARE VERY DULL AND HAVE COMPLAINTS OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. IT DID NOT HAPPEN IN SURGERY. (B)(4) IS RELATED TO (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22542602 ↗MalfunctionJul 18, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS ARE VERY DULL AND HAVE COMPLAINTS OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. IT DID NOT HAPPEN IN SURGERY. (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22542465 ↗MalfunctionJul 18, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS ARE VERY DULL AND HAVE COMPLAINTS OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. IT DID NOT HAPPEN IN SURGERY. (B)(4) IS RELATED TO (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22542263 ↗MalfunctionJul 18, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS ARE VERY DULL AND HAVE COMPLAINTS OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. IT DID NOT HAPPEN IN SURGERY. (B)(4) IS RELATED TO (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22542228 ↗
Other REAMER devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 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
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page