LCS 1278-57-025Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT ROTATING PLATFORM DEEP DISH STD 12.5mm · Class 3 · Implant
All models of LCS (45)
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 10603295020721), received between Jan 29, 2026 and Mar 24, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Naturally Worn” (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.
Reports received per month
Most reported problems
Device problems
- Naturally Worn2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 24, 2026Naturally Worn
IT WAS REPORTED THAT LCS DEEP DISH MB INSERT + LCS COMPLETE PAT NEED TO BE CHANGED DUE TO LENGTH OF STAY AND WEAR. PATIENT HAD PREVIOUSLY HAD AN INLAY CHANGE AND PATELLA RESURFACING IN 2008 OR 2009.
Patient problems: Insufficient Information
MAUDE report 24673733 ↗InjuryJan 29, 2026Naturally Worn
IT WAS REPORTED A LCS RP DD INLAY AND 3 PEG PATELLA NEEDS TO BE CHANGED DUE TO BROKEN POLY AT THE PATELLA. ADDITIONALLY, IMPLANTS ARE WORN OUT, BECAUSE OF LONG IMPLANTATION DURATION. REVISION SURGERY IS PLANNED ON AN UNKNOWN DATE.
Patient problems: Insufficient Information
MAUDE report 24215412 ↗
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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