QUICKSET 2440-00-510Recalls & reported problems

Summary

The FDA's MAUDE database contains 297 adverse event reports that list this exact device (DI 10603295123798), received between Aug 17, 2017 and Sep 18, 2026 — classified as 297 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (77 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 297 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 18, 2026Mechanical Jam

  It was reported that the grater device was too dull, the handles were too stiff, and the coating on the trays was peeling. The event did not occur during surgery. It was reported that during in-house engineering evaluation, it was determined that the device was deformed/bent. All available information has been disclosed.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50819104 ↗
• MalfunctionJun 17, 2026Break

  IT WAS REPORTED THAT THE QUICKSET ACE GRATER HANDLE BROKE AFTER THE SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25536627 ↗
• MalfunctionJun 17, 2026Break

  IT WAS REPORTED THAT THE QUICKSET ACE GRATER HANDLE WAS BROKEN AFTER SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25533045 ↗
• MalfunctionJun 17, 2026Break

  IT WAS REPORTED THAT THE QUICKSET ACE GRATER HANDLE WAS BROKEN AFTER SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25532845 ↗
• MalfunctionApr 3, 2026Break

  IT WAS REPORTED THAT REAMER HANDLE SNAPPED AT THE CONNECTION JUNCTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24778539 ↗
• MalfunctionMar 25, 2026Break

  IT WAS REPORTED THAT THE CONNECTION ON HANDLE POINT BROKE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24691119 ↗
• MalfunctionMar 16, 2026Break; Unintended Movement

  IT WAS REPORTED DURING THE ASSEMBLY OF THE ACETABULAR REAMING BASKET, IT WAS DISCOVERED THAT IT WAS BROKEN. THE SURGEON REAMED, AND THE REAMING BASKET CAME LOOSE. THIS INCIDENT INCREASED THE SURGICAL TIME.

  Patient problems: Insufficient Information

  MAUDE report 24603507 ↗
• MalfunctionFeb 13, 2026Break; Device-Device Incompatibility

  IT WAS REPORTED THAT DURING A TOTAL HIP REPLACEMENT SURGERY, THE GRATER SHAFT TIP WAS BROKEN. THE GRATER WOULD NOT CONNECT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24333891 ↗
• MalfunctionFeb 12, 2026Break

  IT WAS REPORTED THAT REAMER HANDLE TIP WAS BROKEN WHEN REAMING FOR THE CUP. ALL PIECES ARE FOUND, NO DELAY TO THE CASE, NO CONSEQUENCES TO THE PATIENT OR CASE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24327129 ↗
• MalfunctionJan 2, 2026Break

  IT WAS REPORTED THAT ACETABULAR GRATER HANDLE WAS BROKEN. ALL PIECES SEEM TO BE RETRIEVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23943152 ↗
• MalfunctionJul 15, 2025No Apparent Adverse Event; No Apparent Adverse Event

  THE DEVICES WERE REPORTED FOR AN UNKNOWN REASON/MALFUNCTION. IT DIDNT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22511781 ↗
• MalfunctionJul 1, 2025Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE ATTUNE FEMORAL IMPACTOR WAS ONE CRACK AWAY FROM BREAKING. PINN GB OFFSET GRATER HANDLE WAS SEPARATED. QUICKSET ACE GRATER HANDLE WAS TOUGH TO PULL DOWN. QUICKSET ACE GRATER HEAD 51MM WAS DULL. LOCKING SCREWDRIVER BODY HAD PART OF TOP METAL BROKEN. THE EVENTS DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22370414 ↗
• MalfunctionJun 27, 2025Break; Break

  IT WAS REPORTED THAT DEVICE IS BROKEN. THIS EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22350216 ↗
• MalfunctionApr 25, 2025Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT HOSPITAL WILL NOT STERILIZE THESE STYLE HANDLES DUE TO THAT LACK OF BEING ABLE TO DISASSEMBLE THE HANDLE DURING THE STERILIZATION PROCESS. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21908252 ↗
• MalfunctionApr 25, 2025Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT HOSPITAL WILL NOT STERILIZE THESE STYLE HANDLES DUE TO THAT LACK OF BEING ABLE TO DISASSEMBLE THE HANDLE DURING THE STERILIZATION PROCESS. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21908234 ↗
• MalfunctionApr 2, 2025Break; Break

  IT WAS REPORTED THAT THE HANDLE WAS DAMAGED AND NEED TO BE REPLACED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21754107 ↗
• MalfunctionMar 25, 2025Break; Break

  IT WAS REPORTED THAT THE HANDLES ARE BROKEN.

  Patient problems: Insufficient Information

  MAUDE report 21686609 ↗
• MalfunctionMar 12, 2025Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE GRATER SHAFT END WOULD SLIDE DOWN ALL THE WAY TO ACCEPT THE GRATER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21588203 ↗
• MalfunctionJan 23, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

  IT WAS REPORTED THAT THE GRATER HANDLES WERE NOT ABLE TO BE PROPERLY STERILIZED PER SPD DEPARTMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21219016 ↗
• MalfunctionJan 23, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

  IT WAS REPORTED THAT THE GRATER HANDLES WERE NOT ABLE TO BE PROPERLY STERILIZED PER SPD DEPARTMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21219012 ↗
• MalfunctionDec 31, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE QUICK RELEASE MECHANISM WAS STIFF AND DIFFICULT TO MOVE. SURGICAL DELAY WAS UNKNOWN.

  Patient problems: Insufficient Information

  MAUDE report 21047564 ↗
• MalfunctionDec 31, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE QUICK RELEASE MECHANISM WAS STIFF AND DIFFICULT TO MOVE. SURGICAL DELAY WAS UNKNOWN.

  Patient problems: Insufficient Information

  MAUDE report 21047563 ↗
• MalfunctionDec 31, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE QUICK RELEASE MECHANISM WAS STIFF AND IT WAS DIFFICULT TO MOVE. THE SURGICAL DELAY WAS UNKNOWN.

  Patient problems: Insufficient Information

  MAUDE report 21047519 ↗
• MalfunctionDec 31, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE QUICK RELEASE MECHANISM WAS STIFF AND IT WAS DIFFICULT TO MOVE. THE SURGICAL DELAY WAS UNKNOWN.

  Patient problems: Insufficient Information

  MAUDE report 21047516 ↗
• MalfunctionNov 26, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED, THAT PATIENT WAS TO UNDERGO ARTHROPLASTY ON (B)(6) 2024. PRIOR TO THE PATIENT ENTERING THE ROOM. IT WAS NOTICED, THAT THE SPRING PORTION OF THE GRATER HANDLE THAT'S PULLED DOWN TO ATTACH THE GRATER HEAD WAS REALLY STIFF AND HARD TO PULL DOWN FAR ENOUGH TO CHANGE THE GRATER HEAD. THE HANDLE WAS PULLED OFF THE TABLE AND NOT USED. NO BROKEN PIECES OR FRAGMENTS. THERE WAS NO PATIENT CONSEQUENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20782235 ↗