QUICKSET 2440-00-578Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 78mm · Class 1
All models of QUICKSET (66)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 22
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 10603295124252), received between Mar 26, 2018 and Jul 18, 2024 — classified as 22 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (18 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 Cut18
- Adverse Event Without Identified Device or Use Problem3
- Dull, Blunt1
Patient problems
- No Clinical Signs, Symptoms or Conditions21
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 18, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE REAMERS WERE DULL. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19771155 ↗MalfunctionOct 10, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS WERE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15570817 ↗MalfunctionAug 23, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT SURGEON COMPLAINED GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15275385 ↗MalfunctionJun 8, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS SIZE 36-80 WERE DULL AND NEEDED TO BE REPLACED WITH NEW ONES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14634216 ↗MalfunctionMay 6, 2022Failure to Cut; Failure to Cut
THE GRATERS ARE DULL. SURGICAL DELAY UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14295842 ↗MalfunctionMay 6, 2022Failure to Cut; Failure to Cut
THE GRATERS ARE DULL. SURGICAL DELAY UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14295826 ↗MalfunctionMay 6, 2022Failure to Cut; Failure to Cut
THE GRATERS ARE DULL. SURGICAL DELAY UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14295518 ↗MalfunctionNov 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE GRATERS ARE DULL BY THE SALES REP. UPON FOLLOW-UP, ONLY TWO GRATER HEADS WITHIN THE SET WERE IDENTIFIED AS DULL WITHIN THE HEALTHCARE SETTING BY THE SURGEON. THE REMAINING GRATERS WERE RETURNED FOR ROUTINE PRODUCT REPLENISHMENT ONLY AND A FAILURE WAS NOT IDENTIFIED AT THE TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12805145 ↗MalfunctionNov 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE GRATERS ARE DULL BY THE SALES REP. UPON FOLLOW-UP, ONLY TWO GRATER HEADS WITHIN THE SET WERE IDENTIFIED AS DULL WITHIN THE HEALTHCARE SETTING BY THE SURGEON. THE REMAINING GRATERS WERE RETURNED FOR ROUTINE PRODUCT REPLENISHMENT ONLY AND A FAILURE WAS NOT IDENTIFIED AT THE TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12805094 ↗MalfunctionNov 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE GRATERS ARE DULL BY THE SALES REP. UPON FOLLOW-UP, ONLY TWO GRATER HEADS WITHIN THE SET WERE IDENTIFIED AS DULL WITHIN THE HEALTHCARE SETTING BY THE SURGEON. THE REMAINING GRATERS WERE RETURNED FOR ROUTINE PRODUCT REPLENISHMENT ONLY AND A FAILURE WAS NOT IDENTIFIED AT THE TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12805078 ↗MalfunctionJun 2, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11921452 ↗MalfunctionMay 19, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS SIZE 36-80 ARE DULL AND NEED TO BE SHARPENED . NO PATIENT CONSEQUENCES OR SURGICAL DELAYS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11849564 ↗MalfunctionApr 6, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11625426 ↗MalfunctionApr 6, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11625409 ↗MalfunctionApr 6, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11625404 ↗MalfunctionMar 30, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11588832 ↗MalfunctionMar 30, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11588727 ↗MalfunctionMar 30, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11588722 ↗MalfunctionFeb 19, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT REAMERS ARE DULL AND NEED REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11348540 ↗MalfunctionFeb 19, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT REAMERS ARE DULL AND NEED REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11348525 ↗MalfunctionFeb 19, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT REAMERS ARE DULL AND NEED REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11348520 ↗MalfunctionMar 26, 2018Dull, Blunt; Dull, Blunt
IT WAS REPORTED THAT THE SURGEON STRUGGLED AS THE REAMERS WERE BLUNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7369474 ↗
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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