QUICKSET 2440-00-566Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 66mm · 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 during orthopedic surgery. Its 152 adverse event reports include no injuries and no deaths, and many describe graters that fail to cut, become dull over time, or corrode; many say this was noticed outside surgery. In the past 12 months there were none, down from 28 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
- 152
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 152 adverse event reports that list this exact device (DI 10603295124139), received between Sep 21, 2017 and Aug 4, 2025 — classified as 152 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (73 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 Cut73
- Corroded42
- No Apparent Adverse Event19
- Dull, Blunt8
- Material Deformation7
- Naturally Worn6
- Contamination /Decontamination Problem5
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions115
- No Consequences Or Impact To Patient27
- Insufficient Information8
- No Information3
- No Code Available1
Recent adverse event reports
The 25 most recent of 152 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY. (B)(4) AND (B)(4) ARE RELATED TO EACH OTHER. (B)(4) HAS BEEN CREATED FOR CAPTURED ADDITIONAL PRODUCTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22705709 ↗MalfunctionAug 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY. (B)(4) ARE RELATED TO EACH OTHER. (B)(4) HAS BEEN CREATED FOR CAPTURED ADDITIONAL PRODUCTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22704661 ↗MalfunctionAug 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY. (B)(4) ARE RELATED TO EACH OTHER. (B)(4) HAS BEEN CREATED FOR CAPTURED ADDITIONAL PRODUCTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22704418 ↗MalfunctionAug 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY. (B)(4) ARE RELATED TO EACH OTHER. (B)(4) HAS BEEN CREATED FOR CAPTURED ADDITIONAL PRODUCTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22704162 ↗MalfunctionAug 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY. (B)(4) ARE RELATED TO EACH OTHER. (B)(4) HAS BEEN CREATED FOR CAPTURED ADDITIONAL PRODUCTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22703479 ↗MalfunctionAug 1, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22689984 ↗MalfunctionAug 1, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22689983 ↗MalfunctionAug 1, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT THE GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22689979 ↗MalfunctionJul 28, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22638331 ↗MalfunctionJul 28, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME AND NEED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22632103 ↗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 22531377 ↗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 22530852 ↗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 22530835 ↗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 22530822 ↗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 22530800 ↗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 22530790 ↗MalfunctionApr 21, 2025Corroded; Corroded
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THERE WERE RUSTY PINNACLE REAMERS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21874860 ↗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 21517860 ↗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 21517844 ↗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 21517733 ↗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 21517618 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THE ISSUE DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21517183 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THE ISSUE DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21516740 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THE ISSUE DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21516316 ↗MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THE ISSUE DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21516177 ↗
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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