QUICKSET 2440-00-565Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 65mm · 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 attachment. Reports mostly describe graters that became dull, corroded or warped over time, and often say this was noticed outside of surgery. The 159 reports include no deaths and no injuries. No recalls name this device, and reports fell from 25 in the prior 12 months to none in the latest 12 months.
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
- 159
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 159 adverse event reports that list this exact device (DI 10603295124122), received between Sep 21, 2017 and Jul 29, 2025 — classified as 159 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (82 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 Cut82
- Corroded43
- No Apparent Adverse Event20
- Naturally Worn11
- Dull, Blunt8
- Material Deformation5
- Adverse Event Without Identified Device or Use Problem4
- Device Contamination with Chemical or Other Material4
Patient problems
- No Clinical Signs, Symptoms or Conditions119
- No Consequences Or Impact To Patient26
- Insufficient Information14
- No Information2
- No Code Available1
Recent adverse event reports
The 25 most recent of 159 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 22646275 ↗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 22646008 ↗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 22645871 ↗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 22645856 ↗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 22532115 ↗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 22531059 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THE GRATERS ARE DULL AND WARPED; RUSTING WAS ALSO NOTED. THIS DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22530657 ↗MalfunctionJul 17, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THE GRATERS ARE DULL AND WARPED; RUSTING WAS ALSO NOTED. THIS DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22530596 ↗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 22438459 ↗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 22438456 ↗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 22438282 ↗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 22437662 ↗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 22414887 ↗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 22414794 ↗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 22414791 ↗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 22414780 ↗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 21517426 ↗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 21516481 ↗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 21516477 ↗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 21516453 ↗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 21516410 ↗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 21453946 ↗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 20677569 ↗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 20676316 ↗MalfunctionNov 12, 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 20666962 ↗
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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