QUICKSET 2440-00-562Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 62mm · 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 appears in 268 adverse event reports, with no deaths and no injuries. The reports mostly describe graters that have become dull, fail to cut, or show rust and warping, often on older units, and say the problem did not happen during surgery. No reports were filed in the last 12 months, down from 26 in the year 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
- 268
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 268 adverse event reports that list this exact device (DI 10603295124092), received between Sep 18, 2017 and Jul 15, 2025 — classified as 268 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (177 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 Cut177
- Corroded60
- No Apparent Adverse Event25
- Dull, Blunt15
- Naturally Worn13
- Material Deformation7
- Device-Device Incompatibility5
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions205
- No Consequences Or Impact To Patient38
- Insufficient Information22
- No Information3
- No Code Available2
- Not Applicable1
Recent adverse event reports
The 25 most recent of 268 reports, in the reporter's own words as published by the FDA.
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 22509638 ↗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 22509637 ↗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 22509635 ↗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 22509631 ↗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 22508101 ↗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 22508095 ↗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 22438453 ↗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 22437668 ↗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 22184266 ↗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 22183214 ↗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 22131299 ↗MalfunctionMar 24, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER REPEATED USE AND TIME. THE EVENT DID NOT OCCUR DURING A SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21678953 ↗MalfunctionMar 24, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER REPEATED USE AND TIME. THE EVENT DID NOT OCCUR DURING A SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21678407 ↗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 21517331 ↗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 21514977 ↗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 21514660 ↗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 21514595 ↗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 21514285 ↗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 21453803 ↗MalfunctionJan 14, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE INSTRUMENT WAS REPORTED FOR AN UNKNOWN REASON. IT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS IDENTIFIED THAT THE DEVICE HAS ROUNDING OF CUTTING EDGES AND CORROSION PATTERNS ON BOTH INSIDE AND OUTSIDE OF THE CUTTING SURFACE.
Patient problems: Insufficient Information
MAUDE report 21152354 ↗MalfunctionJan 14, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE INSTRUMENT WAS REPORTED FOR AN UNKNOWN REASON. IT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS IDENTIFIED THAT THE DEVICE HAS ROUNDING OF CUTTING EDGES AND CORROSION PATTERNS ON BOTH INSIDE AND OUTSIDE OF THE CUTTING SURFACE.
Patient problems: Insufficient Information
MAUDE report 21152339 ↗MalfunctionJan 14, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE INSTRUMENT WAS REPORTED FOR AN UNKNOWN REASON. IT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS IDENTIFIED THAT THE DEVICE HAS ROUNDING OF CUTTING EDGES AND CORROSION PATTERNS ON BOTH INSIDE AND OUTSIDE OF THE CUTTING SURFACE.
Patient problems: Insufficient Information
MAUDE report 21152326 ↗MalfunctionJan 14, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE INSTRUMENT WAS REPORTED FOR AN UNKNOWN REASON. IT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS IDENTIFIED THAT THE DEVICE HAS ROUNDING OF CUTTING EDGES AND CORROSION PATTERNS ON BOTH INSIDE AND OUTSIDE OF THE CUTTING SURFACE.
Patient problems: Insufficient Information
MAUDE report 21152317 ↗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 20677883 ↗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 20677772 ↗
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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