QUICKSET 2440-00-573Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 73mm · Class 1
All models of QUICKSET (66)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy Quickset reamer is the subject of reports mostly describing dull heads that fail to cut, with a couple mentioning corrosion. There are 25 reports naming its identifier, with no deaths and no injuries. 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
- 25
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 10603295124207), received between Mar 26, 2018 and Jul 22, 2024 — classified as 25 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (19 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Cut19
- Adverse Event Without Identified Device or Use Problem3
- Corroded2
- Dull, Blunt1
Patient problems
- No Clinical Signs, Symptoms or Conditions22
- No Consequences Or Impact To Patient2
- Insufficient Information1
Recent adverse event reports
The 25 most recent of 25 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 19796673 ↗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 19772077 ↗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 16335695 ↗MalfunctionOct 10, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GRATERS ARE DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15572947 ↗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 15275881 ↗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 14634396 ↗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 14288036 ↗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 14288029 ↗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 14287887 ↗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 12805333 ↗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 12805331 ↗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 12805305 ↗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 11921342 ↗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 11849549 ↗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 11625250 ↗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 11625246 ↗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 11625239 ↗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 11582670 ↗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 11582658 ↗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 11582635 ↗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 11348424 ↗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 11348418 ↗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 11348412 ↗MalfunctionDec 26, 2019Corroded; Corroded
EVENT: TRACE OF BLOOD STAINS. WHEN OPENING THIS BOX, THERE WERE TWO SPOTS. AS WE COULD NOT TELL IF IT WAS BLOOD OR RUST, THE HOSPITAL EMPLOYEE USED HYDROGEN PEROXIDE AND THEN THE SURGEON SAID HE DID NOT CONSIDER THAT A STERILE BOX ANYMORE, SO HE SUSPENDED IT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9520504 ↗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 7369456 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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