QUICKSET 2440-00-547Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 47mm · 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 attachment used in surgery. Most of its 1,073 reports describe the grater failing to cut, with staff finding it too dull or chipped during reprocessing. The reports include no deaths and no injuries, and 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
- 1,073
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,073 adverse event reports that list this exact device (DI 10603295123941), received between Aug 16, 2017 and Apr 6, 2026 — classified as 1,073 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (809 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 Cut809
- Dull, Blunt133
- Naturally Worn120
- No Apparent Adverse Event49
- Corroded43
- Break29
- Material Twisted/Bent25
- Adverse Event Without Identified Device or Use Problem15
Patient problems
- No Clinical Signs, Symptoms or Conditions834
- No Consequences Or Impact To Patient167
- Insufficient Information59
- No Information25
- No Code Available17
- Not Applicable7
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 25 most recent of 1,073 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 24793693 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793425 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793424 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793420 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793419 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793417 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793416 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793414 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793413 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793412 ↗MalfunctionApr 6, 2026Break
DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THE 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 REPORTED PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24793409 ↗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 24244225 ↗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 24244224 ↗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 24244223 ↗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 24244222 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24236036 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THE QUICKSET ACE GRATER HEADS WERE NO LONGER SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24235995 ↗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 24207097 ↗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 24202271 ↗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 24198482 ↗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 24198474 ↗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 24198468 ↗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 24198467 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEEDED TO BE REPLACED. DOCTORS COMPLAINED THAT THEY WERE VERY DULL AND STERILE PROCESSING COMPLAINED OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22511520 ↗MalfunctionJul 15, 2025Corroded; Material Deformation; Corroded; Material Deformation
IT WAS REPORTED THAT OLD PINNACLE GRATERS NEEDED TO BE REPLACED. DOCTORS COMPLAINED THAT THEY WERE VERY DULL AND STERILE PROCESSING COMPLAINED OF RUST AND WARPING. THESE ARE OVER 10 YEARS OLD. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22511518 ↗
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 2440-00-555Depuy (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
- 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.
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