QUICKSET 2440-00-564Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 64mm · 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 cutting tool used to shape bone during joint replacement surgery. Many of the 179 reports describe the tool failing to cut or corroding, and several note it did not happen in surgery. The reports include 178 malfunctions, 1 injury and no deaths. There are no reports from the last 12 months, compared with 27 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
- 179
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 179 adverse event reports that list this exact device (DI 10603295124115), received between Sep 21, 2017 and Jul 29, 2025 — classified as 1 injury, 178 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (89 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 Cut89
- Corroded55
- No Apparent Adverse Event19
- Dull, Blunt10
- Material Deformation8
- Naturally Worn7
- Material Twisted/Bent5
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions134
- No Consequences Or Impact To Patient34
- Insufficient Information9
- No Information2
- Not Applicable2
- No Code Available1
Recent adverse event reports
The 25 most recent of 179 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 22645661 ↗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 22645592 ↗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 22645437 ↗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 22645371 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT THE HANDLES NEED REPLACED TO MATCH CROSSBACK GRATERS. IT WAS NOTED THE DEVICES WERE DULL AND THERE WERE ADDITIONAL COMPLAINTS ABOUT RUST AND WARPING. EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL IMPACTED PRODUCTS ARE CAPTURED IN (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22531873 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT THE HANDLES NEED REPLACED TO MATCH CROSSBACK GRATERS. IT WAS NOTED THE DEVICES WERE DULL AND THERE WERE ADDITIONAL COMPLAINTS ABOUT RUST AND WARPING. EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL IMPACTED PRODUCTS ARE CAPTURED IN (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22531821 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT THE HANDLES NEED REPLACED TO MATCH CROSSBACK GRATERS. IT WAS NOTED THE DEVICES WERE DULL AND THERE WERE ADDITIONAL COMPLAINTS ABOUT RUST AND WARPING. EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL IMPACTED PRODUCTS ARE CAPTURED IN (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22531759 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT THE HANDLES NEED REPLACED TO MATCH CROSSBACK GRATERS. IT WAS NOTED THE DEVICES WERE DULL AND THERE WERE ADDITIONAL COMPLAINTS ABOUT RUST AND WARPING. EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL IMPACTED PRODUCTS ARE CAPTURED IN (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22531601 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT THE HANDLES NEED REPLACED TO MATCH CROSSBACK GRATERS. IT WAS NOTED THE DEVICES WERE DULL AND THERE WERE ADDITIONAL COMPLAINTS ABOUT RUST AND WARPING. EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL IMPACTED PRODUCTS ARE CAPTURED IN (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22531566 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT THE HANDLES NEED REPLACED TO MATCH CROSSBACK GRATERS. IT WAS NOTED THE DEVICES WERE DULL AND THERE WERE ADDITIONAL COMPLAINTS ABOUT RUST AND WARPING. EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL IMPACTED PRODUCTS ARE CAPTURED IN (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22530979 ↗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 22438465 ↗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 22438463 ↗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 22438460 ↗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 22437673 ↗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 22415325 ↗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 22414793 ↗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 22414779 ↗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 22414778 ↗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 21517057 ↗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 21516426 ↗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 21516284 ↗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 21516271 ↗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 21516127 ↗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 21453762 ↗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 20677783 ↗
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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