QUICKSET 2440-00-558Recalls & reported problems
Depuy (Ireland) · QUICKSET GRATER HEAD 58mm · 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. Its 655 reports mostly describe the grater failing to cut because it is dull, worn, corroded or chipped, with some reports of cracks in handles. There are no deaths or injuries reported, 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
- 655
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 655 adverse event reports that list this exact device (DI 10603295124054), received between Aug 10, 2017 and May 27, 2026 — classified as 655 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (475 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 Cut475
- Dull, Blunt69
- Naturally Worn68
- Corroded53
- No Apparent Adverse Event26
- Break23
- Adverse Event Without Identified Device or Use Problem20
- Material Deformation12
Patient problems
- No Clinical Signs, Symptoms or Conditions528
- No Consequences Or Impact To Patient98
- Insufficient Information25
- No Information12
- No Code Available9
- Not Applicable4
Recent adverse event reports
The 25 most recent of 655 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 27, 2026Material Deformation
IT WAS REPORTED THAT T-HANDLE FORMED A CRACK WHILE REAMING FOR A SUMMIT STEM. IN ADDITION TO THIS, A QUICKSET GRATER HEAD BENT AT THE COUPLING WHILE INSERTING TO REAM THE ACETABULUM. IN BOTH CASES, NO PIECES BROKE OFF AND SURGICAL TIME WAS NOT EXTENDED. NO ADVERSE CONSEQUENCES FOR THE PATIENT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25302310 ↗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 24837682 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790366 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790356 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790350 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790329 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790304 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790284 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790272 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790254 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24790232 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789964 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789950 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789932 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789919 ↗MalfunctionApr 6, 2026Break
IT WAS REPORTED THE GRATERS WERE DULL AND CHIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24789875 ↗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 24207375 ↗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 24207374 ↗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 24207371 ↗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 24201158 ↗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 24201153 ↗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 24201145 ↗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 24201138 ↗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 24200983 ↗MalfunctionAug 25, 2025Break; Break
IT WAS REPORTED THAT THERE WAS A BROKEN PINNACLE REAMER 58MM. THE METAL COUPLING ON THE REAMER SEPARATED FROM THE REAMER BODY INTO TWO PARTS DURING REAMING. THERE WAS NO SURGICAL DELAY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THERE WERE NO PATIENT CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22884660 ↗
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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