QUICKSET 2440-00-556Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 56mm · 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 tool used to shape bone. Its 817 reports describe malfunctions, with no injuries reported. Most describe the grater failing to cut well, being dull or worn, and some describe chipped or cracked parts. 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
- 817
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 817 adverse event reports that list this exact device (DI 10603295124030), received between Aug 16, 2017 and Aug 3, 2026 — classified as 817 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (575 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 Cut575
- Dull, Blunt114
- Naturally Worn91
- No Apparent Adverse Event44
- Corroded42
- Break29
- Material Twisted/Bent19
- Adverse Event Without Identified Device or Use Problem15
Patient problems
- No Clinical Signs, Symptoms or Conditions625
- No Consequences Or Impact To Patient146
- Insufficient Information37
- No Information21
- No Code Available8
- Not Applicable5
Recent adverse event reports
The 25 most recent of 817 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 3, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50117667 ↗MalfunctionJun 8, 2026No Apparent Adverse Event
IT WAS REPORTED THAT THE REAMERS WERE DULL. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25430459 ↗MalfunctionApr 9, 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. NO OTHER INFORMATION WAS PROVIDED AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24837760 ↗MalfunctionApr 3, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24776814 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762268 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING, THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762267 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762266 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762265 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762264 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762263 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762262 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762258 ↗MalfunctionApr 2, 2026Break
NO FURTHER INFORMATION IS AVAILABLE. ITEMS UNAVAILABLE FOR RETURN. DURING MEDICAL DEVICE REPROCESSING THE STAFF NOTICED THAT THESE GRATERS ARE TOO DULL AND CHIPPED TO BE USED ON A PATIENT. NO PATIENT OR USER HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24762257 ↗MalfunctionMar 10, 2026Break
IT WAS REPORTED THAT THE REAMER BASKET CAME APART. CASE WAS NOT DELAYED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24557521 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT THE ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24235647 ↗MalfunctionFeb 2, 2026Failure to Cut; No Apparent Adverse Event
IT WAS REPORTED THAT THE ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24234014 ↗MalfunctionJan 29, 2026Failure to Cut
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207373 ↗MalfunctionJan 29, 2026Failure to Cut
IT WAS REPORTED THAT SURGEON HAS COMPLAINED ACETABULAR REAMERS ARE NOT SHARP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24207372 ↗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 24200363 ↗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 24200360 ↗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 24200356 ↗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 24200352 ↗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 24200256 ↗MalfunctionNov 16, 2025Break; Break
IT WAS REPORTED THAT THA- BROKEN GRATER WAS FOUND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23565509 ↗MalfunctionJul 22, 2025No Apparent Adverse Event; No Apparent Adverse Event
GRATERS ARE DULL AND TO NEED TO BE REPLACED WITH CROSSBACK GRATERS. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22566767 ↗
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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