QUICKSET 2440-00-568Recalls & reported problems

Summary

The FDA's MAUDE database contains 110 adverse event reports that list this exact device (DI 10603295124153), received between Sep 21, 2017 and Aug 1, 2025 — classified as 110 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (58 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 110 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 1, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22689981 ↗
• MalfunctionAug 1, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22689977 ↗
• MalfunctionAug 1, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22689976 ↗
• MalfunctionJul 28, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22631945 ↗
• MalfunctionJul 28, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22631808 ↗
• MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEEDED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22438556 ↗
• MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEEDED TO BE REPLACED. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22438552 ↗
• MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATER SETS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22435978 ↗
• MalfunctionJul 8, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATER SETS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22435976 ↗
• MalfunctionJul 7, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE INSTRUMENTS HAD AN UNKNOWN ALLEGATION AND NEED REPLACED WITH CROSS BACKS. THE EVENT DID NOT HAPPEN IN SURGERY. DURING MANUFACTURER'S INVESTIGATION OF THE RETURNED DEVICE IT WAS FOUND THAT THERE WAS BLUNTING OF CUTTING EDGES. ADDITIONALLY, CORROSION PATTERNS WERE FOUND BOTH OUTSIDE AND INSIDE OF THE CUTTING SURFACE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22414452 ↗
• MalfunctionMar 19, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21647363 ↗
• MalfunctionMar 19, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21647359 ↗
• MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21518015 ↗
• MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21517869 ↗
• MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATERS HAVE BECOME DULL OVER TIME AND NEED REPLACEMENT. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21517672 ↗
• MalfunctionMar 4, 2025No Apparent Adverse Event; No Apparent Adverse Event

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21517271 ↗
• MalfunctionFeb 25, 2025No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE GRATERS ARE DULL. THE EVENT DID NOT HAPPEN DURING SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21461924 ↗
• MalfunctionOct 10, 2024Material Deformation; Naturally Worn; Material Deformation; Naturally Worn

  ADDITIONAL INFORMATION RECEIVED STATES THAT NO SURGICAL DELAY FOR ANY OF THESE REPORTED DEVICES, HOWEVER, TIME IS REQUIRED TO ORDER LOANER SETS WHILE WAITING FOR MISSING ITEMS TO BE RESTOCKED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20423180 ↗
• MalfunctionSep 9, 2024Corroded; Corroded

  IT WAS REPORTED THAT THE CONSIGNMENT GRATER HEADS ARE RUSTED. ADDITIONAL INFORMATION RECEIVED STATES THAT THIS IS A PRE-OPERATIVE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20171025 ↗
• MalfunctionJul 22, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED, THAT THE INSTRUMENT WAS DULL.

  Patient problems: Insufficient Information

  MAUDE report 19798822 ↗
• MalfunctionJul 22, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE PRODUCTS WERE DULL.

  Patient problems: Insufficient Information

  MAUDE report 19797081 ↗
• MalfunctionJul 18, 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 19772062 ↗
• MalfunctionJun 11, 2024No Apparent Adverse Event; No Apparent Adverse Event

  IT WAS REPORTED THAT THE INSTRUMENT HAS AN UNKNOWN ALLEGATION. THE EVENT DID NOT HAPPEN DURING 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 19509734 ↗
• MalfunctionJun 5, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT GRATERS WERE DULL AND NEED TO BE SHARPENED. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19472274 ↗
• MalfunctionJun 5, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE GRATERS WERE DULL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19472252 ↗