QUICKSET 2440-00-571Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 71mm · 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 reamer used to shape bone during hip surgery. The 28 reports mostly describe blades that would not cut or had gone dull and needed replacing, along with some corrosion and one broken reamer, with most reports noting no effect on the patient. No deaths or injuries were reported, and no reports came in during the past year. 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
- 28
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 28 adverse event reports that list this exact device (DI 10603295124184), received between Mar 26, 2018 and Jul 22, 2024 — classified as 28 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (20 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 Cut20
- Adverse Event Without Identified Device or Use Problem3
- Corroded3
- Break1
- Dull, Blunt1
Patient problems
- No Clinical Signs, Symptoms or Conditions26
- Insufficient Information1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 25 most recent of 28 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 22, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE PRODUCTS WERE DULL.
Patient problems: Insufficient Information
MAUDE report 19796203 ↗MalfunctionJul 18, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT REAMERS WERE DULL. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19772074 ↗MalfunctionMay 10, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT REAMERS WERE DULL. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19285599 ↗MalfunctionJul 28, 2023Break; Break
IT WAS REPORTED THAT THE ACETABULAR REAMER WAS BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17413514 ↗MalfunctionFeb 9, 2023Corroded; Corroded
THE NURSE AT THE HOSPITAL SENT SOME PICTURES OF THE ACETABULAR FRESAS ALLEGING SIGNS OF OXIDATION. THERE WAS NO IMPACT ON SURGERY OR PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16335788 ↗MalfunctionOct 11, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15575072 ↗MalfunctionAug 23, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE SURGEON COMPLAINED GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15275842 ↗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 14634390 ↗MalfunctionJun 7, 2022Corroded; Corroded
IT WAS REPORTED THAT THE GRATERS ARE RUSTY. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14622807 ↗MalfunctionJun 3, 2022Corroded; Corroded
IT WAS REPORTED THAT GRATERS ARE RUSTY. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14598241 ↗MalfunctionMay 5, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ALL GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14287432 ↗MalfunctionMay 5, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ALL GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14287404 ↗MalfunctionMay 5, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT ALL GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14287364 ↗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 12805435 ↗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 12805421 ↗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 12805351 ↗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 11921374 ↗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 11849552 ↗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 11620578 ↗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 11620496 ↗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 11620439 ↗MalfunctionMar 29, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11581891 ↗MalfunctionMar 29, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11581876 ↗MalfunctionMar 29, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11581867 ↗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 11348341 ↗
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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