QUICKSET 2440-00-541Recalls & reported problems

Summary

The FDA's MAUDE database contains 250 adverse event reports that list this exact device (DI 10603295123880), received between Sep 20, 2017 and Jul 22, 2025 — classified as 250 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (170 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.

Most reported problems

Recent adverse event reports

The 25 most recent of 250 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 22, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22565200 ↗
• MalfunctionJul 22, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT GRATERS HAD BECOME DULL OVER TIME AND NEED TO BE REPLACED. THIS EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22565197 ↗
• MalfunctionJul 7, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT ITEMS NEED REPLACED WITH CROSS BACKS. A PRODUCT HAS BEEN REPORTED BUT THE REASON FOR REPORTING IS UNKNOWN. THIS EVENT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS FOUND THAT THE CUTTING EDGES OF THE DEVICE ARE BLUNTING/ROUNDING. ADDITIONALLY SIGNS OF CORROSION WERE OBSERVED AROUND THE CUTTING SURFACE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22414001 ↗
• MalfunctionJun 9, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED INSTRUMENTS WERE REPORTED FOR UNKNOWN ISSUE. IT DID NOT HAPPEN IN SURGERY. (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22171406 ↗
• MalfunctionJun 9, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED INSTRUMENTS WERE REPORTED FOR UNKNOWN ISSUE. IT DID NOT HAPPEN IN SURGERY.(B)(4) IS LINKED TO (B)(4) AND (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22171376 ↗
• MalfunctionJun 9, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED INSTRUMENTS WERE REPORTED FOR UNKNOWN ISSUE. IT DID NOT HAPPEN IN SURGERY. (B)(4) IS LINKED TO (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22171141 ↗
• MalfunctionJun 4, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATERS WERE DULL. THERE WAS NO PROCEDURE OR PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144686 ↗
• MalfunctionMay 14, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT SEVERAL INSTRUMENTS WERE DAMAGED. THE MEDIUM SIZE DRILL BROKE INTO TWO PIECES DURING USE. THE ACETABULAR CUTTERS ARE NOT SHARP.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22017349 ↗
• MalfunctionMar 6, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME WITH REPEATED USE. THE ISSUE DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21539896 ↗
• MalfunctionMar 6, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME WITH REPEATED USE. THE ISSUE DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21539819 ↗
• MalfunctionMar 6, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME WITH REPEATED USE. THE ISSUE DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21539660 ↗
• MalfunctionMar 6, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT GRATERS HAVE BECOME DULL OVER TIME WITH REPEATED USE. THE ISSUE DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21538923 ↗
• MalfunctionSep 10, 2024No Apparent Adverse Event; No Apparent Adverse Event

  THE GRATER HEADS WERE REPORTED FOR AN UNKNOWN REASON.

  Patient problems: Insufficient Information

  MAUDE report 20185641 ↗
• MalfunctionSep 10, 2024No Apparent Adverse Event; No Apparent Adverse Event

  THE GRATER HEADS WERE REPORTED, FOR AN UNKNOWN REASON.

  Patient problems: Insufficient Information

  MAUDE report 20185640 ↗
• MalfunctionSep 3, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL AND NEED REPLACEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20128604 ↗
• MalfunctionSep 3, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL AND NEED REPLACEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20128548 ↗
• MalfunctionSep 3, 2024Corroded; Corroded

  IT WAS REPORTED THAT THE GRATERS ARE RUSTY SO SPD WILL NOT STERILIZE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20127262 ↗
• MalfunctionJul 19, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE PRODUCTS WERE DULL.

  Patient problems: Insufficient Information

  MAUDE report 19781673 ↗
• MalfunctionJul 19, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE INSTRUMENTS WERE DULL.

  Patient problems: Insufficient Information

  MAUDE report 19781420 ↗
• MalfunctionJul 18, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMERS WERE DULL. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19775572 ↗
• MalfunctionJul 9, 2024Failure to Cut; Naturally Worn; Failure to Cut; Naturally Worn

  STAFF HAVE INDICATED THAT THE GRADERS REQUIRE A REPLACEMENT DUE TO WEAR AND TEAR AND BEING DULL OVERTIME. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19702835 ↗
• MalfunctionJun 11, 2024No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE CROSSBACK GRATER WAS REPORTED FOR UNKNOWN REASON. THE EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL EVENT INFORMATION: VISUAL ANALYSIS OF THE RETURNED DEVICE FOUND SIGNS OF WORN OUT AT THE SURFACE OF THE QUICKSET ACE GRATER HEAD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19511318 ↗
• MalfunctionJun 11, 2024No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE CROSSBACK GRATER WAS REPORTED FOR UNKNOWN REASON. THE EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL EVENT INFORMATION: VISUAL ANALYSIS OF THE RETURNED DEVICE FOUND SIGNS OF WORN OUT AT THE SURFACE OF THE QUICKSET ACE GRATER HEAD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19511314 ↗
• MalfunctionJun 11, 2024No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE CROSSBACK GRATER WAS REPORTED FOR UNKNOWN REASON. THE EVENT DID NOT HAPPEN IN SURGERY. ADDITIONAL EVENT INFORMATION: VISUAL ANALYSIS OF THE RETURNED DEVICE FOUND SIGNS OF WORN OUT AT THE SURFACE OF THE QUICKSET ACE GRATER HEAD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19511309 ↗
• MalfunctionMay 16, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT REAMERS WERE DULL. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19336777 ↗