ATTUNE 2544-00-024Recalls & reported problems
Depuy (Ireland) · ATTUNE FEMORAL FINISHING GUIDE SIZE 4 · Class 1
All models of ATTUNE (1475)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295395591), received between Oct 25, 2024 and Nov 19, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (4 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
- Material Deformation4
- Naturally Worn4
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 19, 2025Break; Break
IT WAS REPORTED THAT THE EVENT DID NOT HAPPEN IN SURGERY. FEMORAL FINISHERS SHOWED SIGN OF WEAR, WITH TORN UP EDGES FROM REPEATING CUTTINGS. NEEDED TO REPLACE THOSE THAT HAVE THE MOST WEAR. NO ISSUES TO PATIENT. NO ISSUES TO SURGEON. NO DELAY IN SURGERY. NO BROKEN PIECES TO RETRIEVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23597960 ↗MalfunctionOct 25, 2024Material Deformation; Naturally Worn; Material Deformation; Naturally Worn
SULCUS GUIDES ARE WORN DOWN AND NEED TO BE REPLACED. ENTRY DRILL IS DULL AND NEEDS TO BE REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20535567 ↗MalfunctionOct 25, 2024Material Deformation; Naturally Worn; Material Deformation; Naturally Worn
SULCUS GUIDES ARE WORN DOWN AND NEED TO BE REPLACED. ENTRY DRILL IS DULL AND NEEDS TO BE REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20534031 ↗MalfunctionOct 25, 2024Material Deformation; Naturally Worn; Material Deformation; Naturally Worn
SULCUS GUIDES ARE WORN DOWN AND NEED TO BE REPLACED. ENTRY DRILL IS DULL AND NEEDS TO BE REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20533954 ↗MalfunctionOct 25, 2024Material Deformation; Naturally Worn; Material Deformation; Naturally Worn
SULCUS GUIDES ARE WORN DOWN AND NEED TO BE REPLACED. ENTRY DRILL IS DULL AND NEEDS TO BE REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20533822 ↗
Other INSTRUMENT, CUTTING, ORTHOPEDIC devices
- SIGMA LCS 9505-01-230Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC95 reports
- ATTUNE 2544-00-522Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC58 reports
- SIGMA LCS 9505-01-229Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC56 reports
- SIGMA 2024-40-100Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC43 reports
- ATTUNE 2545-00-158Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC41 reports
- ATTUNE 2545-00-156Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC41 reports
- SIGMA 2024-40-200Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC40 reports
- ATTUNE 2545-00-155Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC39 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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