INTUITION 2525-50-002Recalls & reported problems
Depuy (Ireland) · INTUITION FOR HP PARTIAL FEMORAL PEG DRILL · Class 1
All models of INTUITION (23)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295544678), received between Feb 11, 2026 and Jun 30, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (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.
Reports received per month
Most reported problems
Device problems
- Unintended Movement2
- Failure to Cut1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 30, 2026Unintended Movement
IT WAS REPORTED THAT THE DRILL DOES NOT RUN SMOOTHLY. IT IS WOBBLY. THERE WAS NO PATIENT HARM AND NO SURGICAL DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25666036 ↗MalfunctionJun 30, 2026Unintended Movement
IT WAS REPORTED THAT THE DRILL DOES NOT RUN SMOOTHLY. IT IS WOBBLY. THERE WAS NO PATIENT HARM AND NO SURGICAL DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25666029 ↗MalfunctionFeb 11, 2026Failure to Cut; Material Deformation
IT WAS REPORTED THAT THE FEMORAL AND THE TIBIA LUG DRILLS WERE BOTH SLIGHTLY SKEWED AND HAD A DIFFICULT TIME DRILLING THE HOLES, THE ADAPTER PIECE WORKED FINE WITH ALL OTHER INSTRUMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24317732 ↗
Other BIT, DRILL devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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