QUICKSET 2274-70-500Recalls & reported problems

Summary

The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 10603295109402), received between Jul 24, 2018 and Sep 24, 2026 — classified as 12 malfunctions.

The most frequently reported specific device problem is “Break” (10 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 12 most recent of 12 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 24, 2026Break

  It was reported that drill bit broke when drilling for screw.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50881528 ↗
• MalfunctionJun 1, 2026Break

  IT WAS REPORTED THAT THE INSTRUMENTS WERE BROKEN AND NOT SUITABLE FOR SURGERY. THE ISSUE DID NOT OCCUR DURING SURGERY AND THERE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25355405 ↗
• MalfunctionJun 1, 2026Break

  IT WAS REPORTED THAT THE INSTRUMENTS WERE BROKEN AND NOT SUITABLE FOR SURGERY. THE ISSUE DID NOT OCCUR DURING SURGERY AND THERE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25350838 ↗
• MalfunctionJun 1, 2026Break

  IT WAS REPORTED THAT IT DID NOT HAPPEN IN SURGERY. INSTRUMENTS WERE BROKEN AND NOT SUITABLE FOR SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25348645 ↗
• MalfunctionNov 18, 2024Break; Break

  IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE INSTRUMENTS WERE BROKEN. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20708650 ↗
• MalfunctionNov 18, 2024Break; Break

  IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2024, THE INSTRUMENTS WERE BROKEN. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20708288 ↗
• MalfunctionNov 18, 2024Break; Break

  IT WAS REPORTED THAT ON AN UNKNOWN DATE IN (B)(6) 2024, THE INSTRUMENTS WERE BROKEN. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20708171 ↗
• MalfunctionNov 18, 2024Break; Break

  IT WAS REPORTED THE INSTRUMENT WAS BROKEN. THERE WAS NO PATIENT INVOLVEMENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20707104 ↗
• MalfunctionOct 17, 2022Corroded; Corroded

  IT WAS REPORTED THAT THE DRILL BIT IS RUSTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15618911 ↗
• MalfunctionApr 28, 2022Break; Break

  DRILL BIT BROKE IN HALF DURING SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14237572 ↗
• MalfunctionMay 17, 2019Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT THE 30MM DRILL BIT FOR ACETABULAR SCREWS BROKE WHILE TRYING TO DRILL THE SCREW HOLES IN GRIPTION CUP. THE BROKEN PIECE WAS REMOVED FROM THE FIELD. ALSO, THE 70MM DRILL BIT WAS SEVERELY BENT WHILE TRYING TO DRILL THE SAME SCREW. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8620337 ↗
• MalfunctionJul 24, 2018Break; Break

  IT WAS REPORTED THAT MULTIPLE DRILL BITS WERE BROKEN DUE TO HARD BONE OF PATIENT. NO ISSUES WITH PRODUCT. SURGEON NEED A SCREW.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7714991 ↗