QUICKSETRecalls & reported problems across all models

We found 7 models of QUICKSET by Depuy Orthopaedics, Inc. in the FDA's device registry (GUDID). Together they are named in 3,790 adverse event reports in the FDA's MAUDE database, received between Dec 17, 2015 and Sep 29, 2026 — classified as 15 injuries, 3,775 malfunctions.

The most frequently reported specific device problem is “Break” (2,647 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported QUICKSET problems

QUICKSET models

7 models, most reported first. Each model has its own page with its reports, recalls and device details.

• QUICKSET 2274-25-500

  BIT, DRILL
  1,985 reports
• QUICKSET 2274-35-500

  BIT, DRILL
  770 reports
• QUICKSET 2274-30-500

  BIT, DRILL
  761 reports
• QUICKSET 2274-45-500

  BIT, DRILL
  211 reports
• QUICKSET 2274-54-500

  TEMPLATE
  49 reports
• QUICKSET 2274-70-500

  BIT, DRILL
  12 reports
• QUICKSET 2274-65-000

  BIT, DRILL
  2 reports

Recent QUICKSET adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Material Deformation

  It was reported that drill bit was bent. Calcar reamer was dull. No adverse affects to the patient. No additional information was available.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50932934 ↗
• MalfunctionSep 29, 2026Break

  It was reported that drill was broke when putting through the cup.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50931477 ↗
• MalfunctionSep 25, 2026Material Deformation

  It was reported that the drill bit tip was bent. No adverse affects to the patient. No additional information is available.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50898713 ↗
• MalfunctionSep 24, 2026Break

  It was reported that drill bit tip broke during case.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50886242 ↗
• 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 ↗
• MalfunctionSep 22, 2026No Apparent Adverse Event

  It was reported that on an unknown date, the products had an unknown allegation.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50856911 ↗
• MalfunctionSep 21, 2026Break

  It was reported that during a Total Hip Replacement, the drill bit broke as doctor was drilling screw holes. There was no delays. Nothing left in patient.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50845682 ↗
• MalfunctionSep 21, 2026Material Deformation

  It was reported that during a surgical procedure, the 25mm drill bit bent while drilling for acetabular screw. There was no negative outcome and no surgical delay. All available information has been provided.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50841514 ↗
• MalfunctionSep 18, 2026Break

  It was reported that during a total hip replacement surgery the drill bit broke. All parts were recovered. No patient was harmed. There was no delay in surgery. All available information has been disclosed.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50819433 ↗
• MalfunctionSep 18, 2026Break

  It was reported that during a total hip replacement surgery a drill bit broke while drilling. It broke into two pieces. The broken piece was found and removed from the patient. All available information has been disclosed.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50819256 ↗
• MalfunctionAug 24, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50419266 ↗
• MalfunctionAug 17, 2026Break; Material Deformation; Material Integrity Problem

  It was reported that during a Total Hip Replacement surgical procedure it was observed that the spring portion of the drill bit failed. During in-house engineering evaluation it was determined that the device was deformed/bent and broken into 2 pieces.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50286417 ↗
• MalfunctionAug 14, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50261375 ↗
• MalfunctionAug 11, 2026Material Deformation

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50214953 ↗
• MalfunctionAug 11, 2026Material Deformation

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50214600 ↗

Other Depuy Orthopaedics, Inc. products

• PINNACLE ALTRX98 models · 5,631 reports
• BIOLOX DELTA40 models · 4,995 reports · 1 recall
• PINNACLE182 models · 4,587 reports
• PINNACLE POROCOAT38 models · 2,112 reports
• SUMMIT POROCOAT20 models · 1,646 reports
• PINNACLE GRIPTION57 models · 1,608 reports
• DURALOC93 models · 1,262 reports
• SUMMIT53 models · 697 reports