LCS COMPLETE 1294-12-060Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS COMPLETE RPS Flexion Femoral CEMENTED LRG LEFT · Class 3 · Implant
All models of LCS COMPLETE (117)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295022947), received between Feb 6, 2019 and Dec 6, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 16, 2026.
Most reported problems
Device problems
- Loss of or Failure to Bond2
Patient problems
- Discomfort1
- No Code Available1
- Not Applicable1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 6, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
REVISION OF LCS KNEE COMPONENTS FOR ASEPTIC LOOSENING. THREE COMPONENTS REMOVED. FEMUR, TIBIA AND INSERT.
Patient problems: Discomfort; Pain
MAUDE report 15923455 ↗InjuryFeb 6, 2019Loss of or Failure to Bond; Loss of or Failure to Bond
PATIENT HAD TOTAL KNEE REVISION FOR LOOSE, SUBSIDED TIBIAL COMPONENT. AFTER DETERMINING THERE WAS NO INFECTION PRESENT, ALL ORIGINAL COMPONENTS EXCEPT PATELLA WERE REMOVED & REVISION WAS COMPLETED. FEMORAL & TIBIAL COMPONENT WERE LOOSE AT CEMENT TO IMPLANT INTERFACE. THERE WAS SMALL INSTRUMENT DELAY DURING CASE IN WHICH THE ATTUNE FEMORAL BROACH TRIAL BOLT ENDED UP WITH STRIPPED THREADS WHICH WOULD ALLOW CONNECTION BETWEEN FEMORAL TRIAL & SLEEVE TRIAL. SURGERY CONTINUED ONCE BOLT WAS SWITCHED OUT.
Patient problems: No Code Available; Not Applicable
MAUDE report 8309840 ↗
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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