ATTUNE 1517-10-910Recalls & reported problems
Depuy (Ireland) · ATTUNE KNEE SYSTEM REVISION CRS ROTATING PLATFORM INSERT AOX SIZE 9 10MM · Class 3 · Implant
All models of ATTUNE (1475)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295056362), received between Apr 16, 2024 and Mar 12, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Device Dislodged or Dislocated1
Patient problems
- Joint Laxity2
- Joint Dislocation1
- Loss of Range of Motion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 12, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED WHERE POLY INSERT WAS REMOVED AND REPLACED DUE TO PATIENT BEING UNABLE TO REACH FULL EXTENSION. THE SURGICAL DELAY IS UNKNOWN. DOI: (B)(6) 2022. DOR: (B)(6) 2025. AFFECTED SIDE: UNKNOWN KNEE.
Patient problems: Loss of Range of Motion
MAUDE report 21587965 ↗InjuryApr 16, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED FOR INSTABILITY. PATIENT HAD TOTAL KNEE DONE THIS MORNING. WHILE IN RECOVERY THE PATIENT DISLOCATED HIS KNEE/IMPLANT. HE WAS BROUGHT BACK INTO SURGERY LATER THAT EVENING AND THE 10MM RP CRS INSERT WAS EXPLANTED AND NEW 14MM RP CRS INSERT WAS IMPLANT.
Patient problems: Joint Dislocation; Joint Laxity
MAUDE report 19116769 ↗InjuryApr 16, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED FOR INSTABILITY. PATIENT HAD TOTAL KNEE DONE THIS MORNING. WHILE IN RECOVERY THE PATIENT DISLOCATED HIS KNEE/IMPLANT. HE WAS BROUGHT BACK INTO SURGERY LATER THAT EVENING AND THE 10MM RP CRS INSERT WAS EXPLANTED AND NEW 14MM RP CRS INSERT WAS IMPLANT.
Patient problems: Joint Laxity
MAUDE report 19115370 ↗
Other Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing devices
- ATTUNE 1506-10-005Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing442 reports
- ATTUNE 1506-10-004Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing442 reports
- ATTUNE 1518-20-038Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing3 deaths393 reports
- LCS SIGMA 1294-33-130Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 recall310 reports
- ATTUNE 1518-20-035Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing342 reports
- P.F.C. SIGMA 96-0102Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 death319 reports
- ATTUNE 1518-20-041Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing308 reports
- ATTUNE 1506-10-007Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing284 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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