QUICKSET 2440-00-563Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 63mm · 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 instrument used to shape bone during joint replacement. Its 256 reports mostly describe the grater failing to cut, becoming dull, and corroding or wearing out with age, with some mentioning rust and warping. There were no deaths and no injuries, and reports fell to 0 in the last 12 months from 26 in the 12 months before. 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
- 256
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 256 adverse event reports that list this exact device (DI 10603295124108), received between Sep 21, 2017 and Jul 29, 2025 — classified as 256 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (162 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 Cut162
- Corroded56
- No Apparent Adverse Event23
- Naturally Worn18
- Dull, Blunt12
- Material Deformation7
- Break6
- Device-Device Incompatibility5
Patient problems
- No Clinical Signs, Symptoms or Conditions209
- No Consequences Or Impact To Patient34
- Insufficient Information11
- No Information3
- Not Applicable2
- No Code Available1
Recent adverse event reports
The 25 most recent of 256 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 29, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND REPLACEMENT NEEDED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22645338 ↗MalfunctionJul 29, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND REPLACEMENT NEEDED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22645154 ↗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 22509912 ↗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 22509640 ↗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 22509639 ↗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 22509634 ↗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 22509633 ↗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 22509627 ↗MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22438467 ↗MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22438466 ↗MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22438464 ↗MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22437660 ↗MalfunctionJul 7, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE GRATER SETS HAD BECOME DULL OVER TIME AND NEEDED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22415318 ↗MalfunctionJul 7, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE GRATER SETS HAD BECOME DULL OVER TIME AND NEEDED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22414776 ↗MalfunctionJun 11, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS WERE DULL. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22184153 ↗MalfunctionJun 11, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS WERE DULL. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22183278 ↗MalfunctionJun 3, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE INSTRUMENTS HAD AN UNKNOWN ALLEGATION. THE EVENT DID NOT HAPPEN IN SURGERY. UPON MANUFACTURERS INVESTIGATION IT WAS NOTED THAT THE INSTRUMENT HAS CORROSION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22131331 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21517232 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21516096 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21516048 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21515103 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21514751 ↗MalfunctionFeb 24, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS WERE DULL. THE ISSUE DID NOT HAPPEN IN SURGERY. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED FOR REPORTING. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21453719 ↗MalfunctionNov 13, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THERE WERE DULL ACETABULAR GRATERS. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO PATIENT CONSEQUENCE. THERE WAS NO SURGICAL DELAY DUE TO THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20677572 ↗MalfunctionNov 13, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED ON AN UNKNOWN DATE THE ACETABULAR GRATERS WERE DULL. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20676367 ↗
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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