QUICKSET 2440-00-542Recalls & reported problems

Summary

The FDA's MAUDE database contains 267 adverse event reports that list this exact device (DI 10603295123897), received between Sep 20, 2017 and Jul 22, 2025 — classified as 267 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (174 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 267 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 22565213 ↗
• 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 22414003 ↗
• 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 22171545 ↗
• 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 22171514 ↗
• 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 22144717 ↗
• 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 22144707 ↗
• 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 21542516 ↗
• 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 21541012 ↗
• 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 21540829 ↗
• 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 21539291 ↗
• MalfunctionSep 17, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE ACETABULAR GRATERS HAVE BECOME DULL AND NEED TO BE REPLACED. UNKNOWN SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20242714 ↗
• MalfunctionSep 17, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE ACETABULAR GRATERS HAVE BECOME DULL AND NEED TO BE REPLACED. UNKNOWN SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20242710 ↗
• 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 20185638 ↗
• MalfunctionSep 9, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMERS WERE DULL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20175533 ↗
• MalfunctionSep 6, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMERS WERE DULL. UNKNOWN SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20163387 ↗
• 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 20128582 ↗
• 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 20128561 ↗
• 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 20128549 ↗
• 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 20127248 ↗
• MalfunctionJul 26, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMERS ARE DULL AND NEED TO BE REPLACED WITH SHARP ONES. IT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19840093 ↗
• MalfunctionJul 24, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE REAMERS WERE DULL, AND THE HANDLES DIDN'T FIT.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 19816234 ↗
• MalfunctionJul 19, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE PRODUCTS WERE DULL.

  Patient problems: Insufficient Information

  MAUDE report 19781728 ↗
• MalfunctionJul 19, 2024Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE INSTRUMENTS WERE DULL.

  Patient problems: Insufficient Information

  MAUDE report 19781603 ↗
• 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 19775620 ↗
• 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 19702742 ↗