QUICKSET 2440-00-550Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 50mm · 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, a surgical reamer, appears in 870 adverse event reports. Most describe the grater failing to cut, and staff finding it too dull and chipped to use during cleaning and sterilization. The reports mention no deaths and no injuries. 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
- 870
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 870 adverse event reports that list this exact device (DI 10603295123972), received between Aug 16, 2017 and Apr 6, 2026 — classified as 870 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (640 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 Cut640
- Dull, Blunt131
- Naturally Worn107
- Corroded43
- No Apparent Adverse Event32
- Break29
- Material Deformation11
- Material Twisted/Bent11
Patient problems
- No Clinical Signs, Symptoms or Conditions659
- No Consequences Or Impact To Patient158
- Insufficient Information44
- No Information23
- No Code Available9
- Not Applicable7
Recent adverse event reports
The 25 most recent of 870 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 24793682 ↗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 24777083 ↗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 24777081 ↗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 24777080 ↗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 24763019 ↗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 24763010 ↗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 24763007 ↗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 24763005 ↗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 24763004 ↗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 24763003 ↗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 24763001 ↗MalfunctionFeb 4, 2026Break
IT WAS REPORTED THAT WHILE USING THE 50 GRATER THE PART THAT CONNECTS BROKE OFF LEAVING JUST THE BASKET GRATER IN THE ACETABULUM. DOCTOR WAS ABLE TO GET IT REMOVED WITHOUT DELAY OR ADVERSE AFFECTS TO PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24257457 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24236068 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24236014 ↗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 24233619 ↗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 24207492 ↗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 24202521 ↗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 24199238 ↗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 24199225 ↗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 24198909 ↗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 24198773 ↗MalfunctionJul 16, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEED TO BE REPLACED. THEY ARE REPORTEDLY DULL WITH RUST AND WARPING DURING STERILE PROCESSING THESE ARE OVER 10 YEARS OLD. THE ISSUES DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22520743 ↗MalfunctionJul 16, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEED TO BE REPLACED. THEY ARE REPORTEDLY DULL WITH RUST AND WARPING DURING STERILE PROCESSING. THESE ARE OVER 10 YEARS OLD. THE ISSUES DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22520713 ↗MalfunctionJul 16, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEED TO BE REPLACED. THEY ARE REPORTEDLY DULL WITH RUST AND WARPING DURING STERILE PROCESSING. THESE ARE OVER 10 YEARS OLD. THE ISSUES DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22520694 ↗MalfunctionJul 16, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEED TO BE REPLACED. THEY ARE REPORTEDLY DULL WITH RUST AND WARPING DURING STERILE PROCESSING. THESE ARE OVER 10 YEARS OLD. THE ISSUES DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22520679 ↗
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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