LCS COMPLETERecalls & reported problems across all models
Depuy Orthopaedics, Inc. · 117 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
LCS COMPLETE models — page 2
117 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- LCS COMPLETE 1294-24-617Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-24-620Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-24-725Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-26-041Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-26-060Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-26-063Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-27-061Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-28-030Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-41-040Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-42-050Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 1294-42-070Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 report
- LCS COMPLETE 2294-01-020TEMPLATE1 report
- LCS COMPLETE 2294-24-422TEMPLATE1 report
- LCS COMPLETE 2294-28-040TEMPLATE1 report
- LCS COMPLETE 2294-29-060TEMPLATE1 report
- LCS COMPLETE 9505-02-881TRAY, SURGICAL, INSTRUMENT1 report
- LCS COMPLETE 9505-02-884TRAY, SURGICAL, INSTRUMENT1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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