QUICKSET 2274-65-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295109389), received between Mar 22, 2018 and Mar 1, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 1, 2021Break; Break

  IT WAS REPORTED THAT DRILL BIT BROKE WHILE DRILLING INTO THE POLY. BROKE AT THE CONNECTION OF THE DRILL BIT AND THE SHAFT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11393863 ↗
• MalfunctionMar 22, 2018Break; Break

  IT WAS REPORTED THAT THE 35MM PINNACLE 3.8 DRILL BIT BROKE OFF INTO PELVIS DURING PREPARATION FOR A CUP SCREW. THE SURGEON ELECTED TO LEAVE THE DRILL BIT IN THE PATIENT. THE DRILL BIT WAS DISCARDED BY OR STAFF AFTER THE CASE. NO SURGICAL DELAY. PIECES LEFT IN PATIENT.

  Patient problems: Foreign Body In Patient; No Consequences Or Impact To Patient

  MAUDE report 7361216 ↗