QUICKSET 2440-00-551Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 51mm · 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 surgical reamer head. Most of its 1,150 reports describe malfunctions, mainly grater heads that fail to cut, are dull or chipped, or are worn. The reports include 1 injury and no deaths. Some reports describe staff finding the graters too dull and chipped to use on a patient during reprocessing. 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
- 1,150
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,150 adverse event reports that list this exact device (DI 10603295123989), received between Aug 16, 2017 and Jul 30, 2026 — classified as 1 injury, 1,149 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (857 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 Cut857
- Dull, Blunt166
- Naturally Worn144
- Corroded43
- No Apparent Adverse Event38
- Material Twisted/Bent33
- Break32
- Material Deformation17
Patient problems
- No Clinical Signs, Symptoms or Conditions878
- No Consequences Or Impact To Patient201
- Insufficient Information61
- No Information25
- No Code Available14
- Not Applicable7
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 25 most recent of 1,150 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 30, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50086516 ↗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 24793684 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791973 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791964 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791619 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791584 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791568 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791562 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791539 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791530 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791524 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791513 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791499 ↗MalfunctionMar 23, 2026Break
IT WAS REPORTED THAT UPON INSPECTION, SETS WERE BROKEN. HOSPITALS HAVE COMPLAINED ABOUT BROKEN INSERTS/PANS AND FLAGGED FOR STERILIZATION. DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24666418 ↗MalfunctionMar 4, 2026Break; Crack
IT WAS REPORTED THAT GRATER WAS BROKEN CRACK ON SIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24506242 ↗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 24233724 ↗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 24207493 ↗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 24207489 ↗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 24202553 ↗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 24199348 ↗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 24199341 ↗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 24199303 ↗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 24199289 ↗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 22520878 ↗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 22520860 ↗
Other REAMER devices
- 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
- 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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