ATTUNE 2513-14-060Recalls & reported problems
Depuy (Ireland) · ATTUNE KNEE SYSTEM REVISION PRESS-FIT STEM TRIAL 14mm x 60mm · Class 1
All models of ATTUNE (1475)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295438830), received between Sep 15, 2023 and Sep 15, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
Device problems
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2023Break; Break
IT WAS REPORTED THAT WHILE REMOVING THE BROACH AND STEM, THE STEM SNAPPED OFF STAYING IN THE TIBIA. THE STEM WAS REMOVED AND ALL BROKEN PIECES WERE RECOVERED. THERE WAS NO SURGICAL DELAY.
Patient problems: Insufficient Information
MAUDE report 17759369 ↗
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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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