QUICKSET 2440-00-545Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 45mm · 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 used to shape bone. The 947 reports mostly describe graters that fail to cut and are dull, chipped or worn, some found by staff during reprocessing. The reports include no deaths and no injuries, and no recalls name this device. Reports rose to 28 over the last year from 14 in the year before.
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
- 947
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 947 adverse event reports that list this exact device (DI 10603295123927), received between Aug 11, 2017 and Apr 6, 2026 — classified as 947 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (703 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 Cut703
- Dull, Blunt109
- Naturally Worn101
- Corroded52
- Break39
- No Apparent Adverse Event34
- Material Twisted/Bent24
- Crack13
Patient problems
- No Clinical Signs, Symptoms or Conditions723
- No Consequences Or Impact To Patient155
- Insufficient Information65
- No Information23
- No Code Available16
- Not Applicable6
Recent adverse event reports
The 25 most recent of 947 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793697 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24792419 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24792418 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24792414 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24792412 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24792405 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THAT DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. THE SUMMIT BROACH HANDLE CLASPS NO LONGER TIGHTEN SUFFICIENTLY ON THE BROACHES. THE EXCEL T HANDLES ARE CRACKED ON THE HANDLE. THE CUP INSURERS ARE CROSS THREADED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24792403 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791947 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791895 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791858 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791848 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791830 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791826 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791816 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24791813 ↗MalfunctionFeb 3, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT ALL GRATERS ARE DULL AND NEED REPLACED OR SHARPENED. WILL SEND BACK AS SOON AS I RECEIVE SHARP REPLACEMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24244232 ↗MalfunctionFeb 3, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT ALL GRATERS ARE DULL AND NEED REPLACED OR SHARPENED. WILL SEND BACK AS SOON AS I RECEIVE SHARP REPLACEMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24244231 ↗MalfunctionFeb 3, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT ALL GRATERS ARE DULL AND NEED REPLACED OR SHARPENED. WILL SEND BACK AS SOON AS I RECEIVE SHARP REPLACEMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24244230 ↗MalfunctionFeb 3, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT ALL GRATERS ARE DULL AND NEED REPLACED OR SHARPENED. WILL SEND BACK AS SOON AS I RECEIVE SHARP REPLACEMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24244226 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED THAT THE ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24233376 ↗MalfunctionJan 29, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207105 ↗MalfunctionJan 29, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207104 ↗MalfunctionJan 29, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS WERE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207102 ↗MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24202136 ↗MalfunctionJan 28, 2026Failure to Cut
IT WAS REPORTED THAT THE ACETABULAR GRATERS IN THE HOSPITALS SETS ARE IN NEED OF SHARPENING AND THEY ARE NO LONGER FUNCTIONING AS EXPECTED. NO KNOWN PATIENT HARM THE FOLLOWING COMPLAINTS ARE LINKED TO CAPTURE ALL IMPACTED PRODUCTS: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24198446 ↗
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 2440-00-552Depuy (Ireland) · REAMER888 reports
- QUICKSET 2440-00-550Depuy (Ireland) · REAMER870 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.
How reports and recalls are matched · Editorial policy · Report an error on this page